BD (Becton, Dickinson and Company) is a global medical technology company that is focused on improving drug deliveryen-us/view/client/becton-dickinson/images/banner-combined.gifwww.bd-careers.com720
Description

Repair and maintain the automated manufacturing equipment in a high volume environment. Troubleshoot and diagnose manufacturing equipment malfunctions and make the necessary repairs. Assist the Manufacturing Engineers with assembly, setup, debugging and installation of automated machinery. Provide drafting support on machine design projects. Provide leadership and training to other senior maintenance personnel this position requires strong leadership skills, operating in an environment without supervision.

1. Lead the maintenance personnel to provide maintenance support for the Manufacturing equipment.

2. Coordinate maintenance activities including emergency maintenance, preventative maintenance, Total Productive Maintenance, and any other projects.

3. Maintain electronic and mechanical devices and repair or replace broken or defective components and mechanisms.

4. Operate electronic and mechanical devices required to troubleshoot manufacturing equipment and make the necessary repairs and/or adjustments.

5. Read electronic and mechanical schematics to resolve both electronic and mechanical issues.

6. Train the less senior maintenance personnel to resolve maintenance electronic and mechanical issues.

7. Work with the Manufacturing Engineers and engage in the machine component and mechanism redesign and assembly, set-up, debugging and installation of equipment. Transfer of equipment to offshore plants and provide training at that plant.

8. Comply with all company policies regarding safety, Good Manufacturing Practices and ISO-9001.

9. Support the production and engineering teams by providing technical assistance with both electronic and mechanical issues.

10. Provides drafting support on machine design projects.

11. Utilize Lock Out Tag Out procedures as required.

12. Comply with all local, state, federal, and BD safety regulations, policies, and procedures including RCRA Hazardous Waste regulations.

13. Comply with all local BD quality policies, procedures, and practices through consistent application of sound quality assurance principles.

14. Other duties as assigned.

Qualifications

Minimum Education:
A.S./A.A. degree in manufacturing technology or equivalent experience.
Minimum Experience:
Seven to ten (7 to 10) years of maintenance support experience in a high-volume, manufacturing environment. Must demonstrate knowledge in inventory systems and be knowledgeable in electro-mechanical devices for high-volume, automated manufacturing equipment and systems.

Job
Manufacturing

Primary Location
US-Utah-Sandy

Shift
Second Shift / Afternoon Start

Relocation Available
No]]>http://www.bd-careers.com/job/SANDY-Sr.-Electro-Mechanic-Jobs-UT-84070/610366/6103666103662010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

JOB SUMMARY:

Responsible for designing, developing, and sustaining optical, and opto-electromechanical systems for diagnostic medical microbiology and molecular instrumentation. Works closely with Electrical, Mechanical, Systems and Software Engineering associates as a member of a project team. Independently evaluates and applies engineering principles to fulfill project objectives. Collects, analyzes, interprets, and reports on data. Presents results to others. Design, develop, and execute optical subsystems with minimal supervision. Acts independently, provides guidance and work assignments to less experienced technicians and engineers.

DUTIES AND Responsibilities:


· Develop design input (specifications) for optical systems in instrumented products.

· Lead or be in sole responsibility for the detail design of optical subsystems.

· Apply engineering principles, analytical skills, and empirical methods to develop statistically robust designs.

· Design products to meet cost targets. Prepare cost estimates of components and assembly labor.

· Accurately estimate work effort for specific engineering tasks for schedule allocation of optical engineering resources.

· Lead, contribute to, and participate in design reviews. Thoroughly assess the ability of proposed designs to meet specified requirements, including manufacturability.

· Assist in test planning and development to insure instrument systems and sub-systems conform to requirements on reliability and robustness.

· Complete assignments within established schedules and budgets.

· Interact closely with mechanical, electrical, systems, and software engineering functions to develop comprehensive solutions to design problems.

· Conform to the requirements of ISO 9001 and CGMP standards for the design and development of medical devices.

Qualifications

EXPERIENCE:

Optical design experience on fluorescence based detection systems. Hands-on experience effectively resolving design, manufacturing, and vendor issues associated with tightly specified parts, component variability and obsolescence. Optics knowledge and experience are required in the following areas:

¨ LED's: specifications, construction, test & burn-in methods

¨ Optical filters: characteristics, coatings, specifications, test & evaluation methods

¨ Thermal characteristics of optical detection devices.

¨ Spectral analysis, imaging optics, and alignment methods

¨ Integration effects of components

¨ Fiber optics: construction, specification, evaluation & test methods

¨ Knowledge and experience in both sequential and non-sequential ray tracing software.

¨ Knowledge of process and tolerance capability of lenses and optical components

¨ Knowledge of fluorescence standards and calibration

¨ Familiarity with digital, analog, electronic circuits design, particularly weak opto-electric signal detection, and troubleshooting is desirable.

MINIMUM Qualifications:


B.S. in optical engineering , mechanical engineering, electric engineering or physics with 5+ years related optical design experience. or M.S in optical engineering , mechanical engineering, electric engineering or physics with 3+ years related optical design experience.

Job
New Product Development

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/BALTIMORE-R-26D-Sr.-Optical-Engineer-Jobs-MD-21201/610396/6103966103962010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The Quality Engineer will be responsible for working closely with other functions within the organization (Manufacturing, R&D, Quality, Engineering, Procurement, Marketing) and ensuring the quality of the product and processes for the assigned product line(s) are in compliance with standard Quality practices. The QE will develop, modify, apply and maintain quality standards and protocols and may also be responsible for developing and implementing strategic quality plans, master validation plans, validation protocols, inspection plans and quality/regulatory compliance operating procedures to meet FDA (Food and Drug Administration) and ISO (International Organization of Standardization) requirements. Responsible for developing, documenting and/or maintaining design history files.

Roles and Responsibilities

· Develop, and maintain the Quality System for BDBAB Miami in compliance with 21 CFR 210/211 and ISO 9001 requirements.

· Work closely with BDBAB Quality staff to correct new and recurring quality / technical issues within Operations using problem solving techniques.

· Develop test instructions, standard operating procedures.

· Assist in the development and review of technical transfer report templates, technical reports and external presentations / publications.

· Provide quality systems training to BDBAB Quality and Operations associates.

· Assist QMRC in quality audits of supplier/Vendors, internal audits and help support Customer Audits. R&D lab reports and results and report back to Quality Management.

· Represents/assists BDBAB Quality in complaint resolutions, product investigations and new product development / operational excellence projects.

· Assists with development and implementation of design history files per GPDS guidelines. Develop and review Quality procedures and facility Commissioning protocols, IQ/OQ and PQ protocols and reports.

· Acts as subject manner expert in all quality and regulatory matters for Operations.

· Performs other duties, projects, as assigned.

Qualifications

Knowledge and Skills

* Understanding of continuous improvement methodologies including lean, six sigma, and validation.
* Knowledge of manufacturing processes and relevant statistical techniques (Six Sigma, Statistical Process Control (SPC).
* Basic to intermediate proficiency in Microsoft Office and statistical programs (i.e. MiniTab, SAS).
* Thorough knowledge of quality system regulations/requirements (i.e. ISO-International Organization for Standardization, FDA-Food and Drug Administration, GMP-Good Manufacturing Practices, EPA- Environmental Protection Agency).
* Effective communication skills at all levels both written and verbal.
* Effective skills in analytical thinking and problem solving.
* Ability to perform multiple tasks and ability to effectively manage conflict.
* Ability to work in teams to obtain results, self motivated/directed, ability to organize and supervise people and activities, minimal supervision required.

Education and Experience

* BS degree in Life Sciences, Engineering (Biology, Chemistry, Microbiology, Electrical, Mechanical, Software/Computer Science) and a minimum of 5-6 years of experience in Pharmaceutical/Biotechnology Industry required.
* Professional certification is preferred (i.e. CQA-Certified Quality Auditor, CQE-Certified Quality Engineer, SQE-Sofware Quality Engineer, CQM-Certified Quality Manager, etc.).
* SAP experience preferred.

Job
Quality Engineering

Primary Location
US-Florida

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Quality-Engineer-Jobs-FL/610448/6104486104482010-04-10BDfull-timeUSDstarting0BSUS-Florida
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Automation Technician II has general responsibility for the installation, maintenance, inspection, and modification of all BD-Wilson site automation equipment, technologies, and processes to include record and control generating operations. He/She is responsible for installation, removal, repair, troubleshooting, calibration, and preventative maintenance of electro-mechanical packaging, utilities, laboratory and warehousing systems. The technician will perform his/her work in a cGMP consistent manner. The technician must be able to work both independently and as a team member. Considerable independent judgment and initiative is required to solve challenging workplace problems. The technician will (a) repair and calibrate using precision measuring instruments, hand and or power tools, electrical repair or modification tools, (b) troubleshoot and repair using manuals, SOPs, specifications, and other workplace aids, (c) complete corrective actions and preventative actions to include predictive maintenance, (d) actively communicate with others to include workplace teams, (e) prepare documents to include maintenance, quality, production, CCRs and other documents/reports as deemed appropriate, (f) communicate status of work assignments as requested, (g) promote safe work practices, (h) complete assigned training, (i) train/mentors new and existing personnel as required, (j) participate in workplace continuous improvement projects, (k) monitors the work of others to include contracted vendors, (l) schedules and organizes work methods, materials and parts, (m) other duties as assigned by Area Management.

Qualifications

Required Skills and Knowledge - Associates Degree or Licensed Journeyman with minimum of 5 years of work experience in pharmaceutical manufacturing environment. Must demonstrate sufficient knowledge of controls and control systems to include SCADA, PLC, Cognex Vision, GE Fanuc Robotics, AB Frequency Drives and BMS. Regularly demonstrates effective work planning skills. Able to contribute to cross functional teams. Medium-Heavy work; exerting up to 75 pounds of force occasionally and/or up to 35 pounds of force frequently, and/or up to 20 pounds of force constantly to move objects. Must be willing to work multiple shifts.

Technical Area of Expertise - Installation, maintenance and modification of equipment to include aseptic filling, high speed packaging, automated warehousing, and plant utilities.

Job
Technician

Primary Location
US-North Carolina-Wilson

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/WILSON-Automation-Technician-II-Jobs-NC-27893/610482/6104826104822010-04-10BDfull-timeUSDstarting0BSWilson, NC, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

PURPOSE & OBJECTIVE

The Project Engineer - Packaging is responsible for identifying and executing equipment and materials selection projects for the packaging of medical consumables. Specifies, procures, and completes projects to introduce new packaging equipment, reduce packaging cost, and improve packaging systems. Projects may focus on existing materials and equipment, the packaging of new products, or the improvement to packaging of existing products. Also provides hands-on technical support for existing packaging equipment and packaging configurations and acts as a liaison with segment R&D personnel on market acceptance of proposed packaging solutions.

Manage projects from concept to implementation, including defining project scope, determining required resources, establishing equipment specifications, providing system startup services, developing processes and executing validation protocols. Ensures compliance/improvement of quality systems in manufacturing (i.e. ISO, QSR, GMP).

Participate in new product development and process improvement projects as a core team member. Interface with suppliers and internal customers (QA, Purchasing, R&D, Marketing, Manufacturing Engineering, Warehouse and Sterilizer) to resolve packaging issues.

ESSENTIAL JOB FUNCTIONS

Lead packaging equipment upgrades on existing equipment. Work with representatives from operations, maintenance/facilities and quality engineering to justify, specify, procure, install, and validate new packaging equipment or improvements to existing equipment. Work with vendors on packaging equipment improvement projects.

Manage capital equipment projects from concept through implementation. Develop technical specifications and bid documents for the procurement of packaging equipment. Issue capital appropriations requests and manage project budgets and schedules. Working with vendors and quality engineering, manage projects from inception through validation to ensure that all performance specifications are met. Supervise the FAT, installation, startup, testing and debug of new or modified packaging equipment. Develop and execute equipment qualification and validation protocols.

Provide technical knowledge of packaging materials and support operations with packaging material concerns. Develop and maintain packaging material specifications. Develop and execute test protocols for packaging material evaluation, validation, and package integrity. Develop and document pallet patterns and develop packaging assembly drawings using software. Proof print plate and other packaging graphics. Transfer packaging designs from research to development to manufacturing and document packaging designs and packaging work instructions.

Lead packaging material rationalization and optimization efforts. Conceive and lead packaging materials cost savings projects through to PQ.

Provide technical support of and perform hands-on troubleshooting and process improvements to packaging equipment in manufacturing operations. Use root cause analysis to eliminate process problems. Train manufacturing engineers and technical support personnel as needed on packaging machinery operations and maintenance.

Improve process reliability of existing packaging equipment. Recommend and implement changes to packaging equipment for quality and productivity enhancements.

Ensure compliance/improvement of quality systems in manufacturing (i.e. ISO, QSR, GMP).

KNOWLEDGE, SKILLS, AND ABILITIES

Project management and leadership skills.

Understanding of packaging equipment, packaging materials and current packaging technologies. Hands-on mechanical troubleshooting. Experience troubleshooting packaging materials issues.

Mechanical and electrical integration experience a plus.

Experience with Process Validation and Statistical Analysis.

Must possess excellent interpersonal, communication, documentation, presentation and computer skills (MS Office, MS Project, MS Excel, MS Powerpoint). Experience with packaging design software such as Freehand, PKG, TOPS, or CAPE desired.

Works in a team based environment and exchanges technical information with management, technical support personnel, and equipment vendors.

Must be self directed and resourceful, detail oriented and able to manage multiple priorities. Must be results driven and action oriented.

Must be able to influence individuals without supervisory authority and motivate others within an extended project team that includes outside contractors and vendors.

Experience with the following packaging materials:

· Top web materials (printed and unprinted, plastic and paper)

· Bottom web materials (flexible and rigid, preformed and unformed)

· Corrugate

· Paperboard

· Poly bags

· Ink

· Labels

Experience with the following packaging equipment:

· Form / Fill / Seal

· F/F/S tooling

· Stretch wrap

· Case Sealer

· Material Handling

· Label Printers and Print and Apply Systems

· Case Erectors

· Tray Sealers

· Labelers

· Bag heat sealers

SUPERVISORY RESPONSIBILITIES

Manages activities of others on project team to achieve program schedules and milestones. Gives direction to other technical resources during project and troubleshooting activities.

WORKING CONDITIONS

Performs job duties in a normal office environment and on the manufacturing floor. Adheres to site safety policies, and quality/business system policies and procedures as applicable.

Must have physical ability to lift up to 65 pounds non-repetitively.

Exposed to fumes and high frequency noise in manufacturing areas.

Safety glasses, hair covering and hearing protection are required on the manufacturing floor and other designated areas.

Occasional travel required to support assigned project needs.

Qualifications

MINIMUM QUALIFICATIONS

BS in Packaging Engineering, Mechanical Engineering, or related engineering curriculum

A minimum of three years of post-college experience in packaging design, specification, or implementation in a high-volume manufacturing environment. Packaging Engineering experience in the medical device or pharmaceutical industry is preferred.

A minimum of three years experience in project leadership from initial concept through project completion.

Job
Manufacturing Engineering

Primary Location
US-North Carolina-Durham

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/DURHAM-Project-Engineer-Packaging-Job-NC-27701/619361/6193616193612010-04-10BDfull-timeUSDstarting0BSDurham, NC, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The Manufacturing Business Team Lead - Biologics works out of the Woburn, MA office and is responsible for the supervision of production team for the manufacture of biologically based products. This position directs and coordinates the operation of the team, with responsibility for results in timely execution of production plan. The Team Lead supports the implementation of lean manufacturing processes and continuous improvement projects. This role interacts with R&D, Marketing, Finance and Quality Assurance to meet strategic goals for new product transfer and drives implementation of continuous improvement, lean manufacturing and inventory management processes throughout plant. Individual is responsible for driving a high performance culture.

Qualifications

KNOWLEDGE AND SKILLS

Demonstrated ability to motivate and manage exempt and non-exempt level personnel.

Knowledge of ERP systems, lean manufacturing procedures, inventory management and Six Sigma principles.

Demonstrated knowledge of project management tools and principles of team leadership.

Demonstrated success working with teams and resolving conflict.

Working knowledge of ISO guidelines.

Effective oral and written communication skills, to include training and presentation skills.

Effective organization, planning skills and interpersonal skills.

Effective science, analytical, technical and problem solving skills.

Ability to lift 35 lbs.

Computer literacy required; i.e. PC software, databases, documentation software.

Bachelors degree required. Minimum of 3 years of demonstrated supervisory experience in manufacturing operation is required. Background in the biological sciences preferred. 1-3 years experience in regulated manufacturing environment is required.

Job
Manufacturing

Primary Location
US-Massachusetts-Woburn

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/WOBURN-Manufacturing-Business-Team-Lead-Biologics-Job-MA-01801/619364/6193646193642010-04-10BDfull-timeUSDstarting0BSWoburn, MA, US
BD, a leading global medical technology company that manufactures and sells medical devices, instrument systems and reagents, is dedicated to improving people's health throughout the world.
BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 27,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public. For more information, please visit www.bd.com.

About us

Description

BD Medical - Pharmaceutical Systems has a heritage of rewarding results with more responsibility and clear accountability. Over the past decade, our business has consistenlty delivered double-digit growth and has a tremendous future. BD Medical -Pharmaceutical Systems, working in partnership with the pharmaceutical industry, develops an array of drug delivery systems that are critical to the integrity and delivery of medicine. Our products facilitate vaccination and therapy against disabling diseases improving the patient and caregiver's experience with medical care and protecting our families. We are proud of doing our part to further BD's mission to help all people live healthy lives.

We are currently seeking a Core Team Leader-Program Manager at our headquarters in Franklin Lakes, NJ. This position will provide expert engineering skill to the business and will also:

• Plan and lead cross-functional product development projects, from concept to manufacturing.

• Lead cross-functional planning, coordination, and reviews.

• Maintain an overview of relevant technologies and products.

• Collaborate in the evaluation and assessment of competitive products, processes or new trends.

• Ensure compliance with BD quality policies, procedures, and practices through appropriate communication, training,

and education of sound quality assurance principles.

• Ensure compliance with all local, state, federal, and BD safety regulations, policies, and procedures.

• Serve as Core Team Leader for world-wide R&D projects

Qualifications

Requirements for this role include:

BS Engineering, preferably mechanical or Biomedical and experience in product development. Advanced Degree preferred.

Minimum 8-15 years of experience in engineering preferably in the pharmaceutical and/or medical device industry

PMP certification preferred

Successful track record of delivering products to market or developing commercially viable technology.

Demonstrated high level skills in project management and product development process

Ability to proactively interact and lead interdisciplinary teams representing all aspects of product development including R&D, QA, RA, Clinical, Finance and Marketing.

High level of interpersonal skills as well as excellent communication and presentation skills

Ability to proactively interact with vendors, management, manufacturing plants and technical staff

Excellent analytical and problem solving skills.

The successful candidate will demonstrate independent thought and judgement in developing methods, techniques and evaluation criteria. A clear understanding of quality, regulatory and clinical standards is a plus.

Job
Mechanical Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Core-Team-Leader-Job-NJ-07417/619373/6193736193732010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
About BD
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

About us

Description

The Associate Medical Director, Medical Affairs BD Medical Surgical Systems (BDMSS) supports the Medical Director for BDMSS in a variety of tasks at the interface between the business, Core product development teams, and the clinical environment. The Associate Director supports the Global Product Development System, providing input into product concepts and specifications, assisting in the design of the Medical Affairs strategy, evaluating the adequacy of proof of product safety and efficacy; reviewing the evidence to support product labeling including, but not limited to, advertising, graphics and instructional materials; and overseeing the preparation of competent medical analyses of safety and efficacy issues related to BDMSS products. The Associate Director supervises BDMSS Medical Specialists and should have professional standing and communication skills appropriate to represent Becton Dickinson to the public and to health care professionals.

Managerial Responsibilities:

Directly supervise and develop selected Medical Specialists including hiring and performance review.
Assist in developing and monitoring of the department budget.

Global Product Development Process:
Serve as a member of key Product Development Core Teams and/or Sustaining Engineering Teams.

Serve as a member of one or more Business Platfoms.
Collaborate with the Medical Director, BDMSS, the Director of Clinical Research and the Medical Specialists to author the Medical Affairs Strategy and Clinical Plan.
Responsible for Medical Affairs review of BDMSS PDNs within their area of responsibility, and for determination of evaluations required for product Medical Affairs release.
Act as an internal consultant on clinical issues relevant to medical devices.
Prepare persuasive, factual reports to support decision-making, project initiations, and regulatory filings.

Safety and Efficacy Evaluations:
Authoritatively represent the viewpoint of health professionals and patients on issues related to the safety and efficacy of medical devices.
Review selected product complaints and MDRs for potential health hazards.
Participate in the development of Health Hazard Analyses.
Assist in developing and executing action plans related to product complaints and defects.

Clinical Education
Assist in the training of BD Associates worldwide, allowing them the opportunity to see and understand clinical practice needs.
Write clinical scientific papers and white papers related to the use of BD products in the delivery of patient care.
Attend key conferences to sense new directions in medical care relevant to medical device use and/or needs and to represent BD interests to the medical community.
Maintain clinical knowledge of current practice and problems associated with the use of BD devices.

Qualifications

The Associate Director, Medical Affairs BDMSS must have an MD degree. Education in the areas of experimental design, statistics, technical writing, product development, and management also enhance the individual's ability to fill this job. The international scope of BD makes foreign language ability an asset. At a minimum, the Associate Director must have an appreciation of cultural differences and an interest in working with international issues.

A minimum of four years of Clinical experience is required. In addition, experience managing and motivating others, international experience, research experience, and accomplishments that demonstrate technical ability and creativity all enhance the individual's value in this managerial position that requires flexibility and innovation.

Job
Other

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Associate-Medical-Director,-Medical-Affairs-Job-NJ-07417/619400/6194006194002010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

Working out of the Woburn, MA office, this position works closely with other functions within the organization (Manufacturing, R&D, Quality, Engineering, Procurement, Marketing) and is responsible for ensuring the quality of the product and process for the assigned product line(s). Develops, modifies, applies and maintains quality standards and protocols. May be responsible for developing and implementing strategic quality plans, master validation plans, validation protocols, inspection plans and quality/regulatory compliance operating procedures to meet FDA (Food and Drug Administration) and ISO (International Organization of Standardization) requirements. May be responsible for developing, documenting and/or maintaining design history files.

Qualifications

* Thorough knowledge of quality system regulations/requirements (i.e. ISO-International Organization for Standardization, FDA-Food and Drug Administration, GLP / GMP-Good Lab / Manufacturing Practices, QSR-Quality System Regulation, EPA- Environmental Protection Agency).
* Effective communication skills at all levels both written and verbal.
* Effective skills in analytical thinking and problem solving.
* Ability to perform multiple tasks and ability to effectively manage conflict.
* Ability to work in teams to obtain results, self motivated/directed, ability to organize and supervise people and activities, minimal supervision required.
* Knowledge of manufacturing processes and relevant statistical techniques (Six Sigma, Statistical Process Control (SPC).
* Basic to intermediate proficiency in Microsoft Office and statistical programs (i.e. MiniTab, SAS).
* Understanding of continuous improvement methodologies including lean, six sigma, and validation.
* Professional certification is preferred (i.e. CQA-Certified Quality Auditor, CQE-Certified Quality Engineer, SQE-Software Quality Engineer, CQM-Certified Quality Manager, etc.).
* SAP experience preferred.
* BS degree is required, preferably in Life Sciences, Engineering (Biology, Chemistry, Microbiology, Electrical, Mechanical, Software/Computer Science).

Job
Quality Engineering

Primary Location
US-Massachusetts-Woburn

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/WOBURN-Quality-Engineer-Job-MA-01801/619405/6194056194052010-04-10BDfull-timeUSDstarting0BSWoburn, MA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Responsible for providing on-site support to BD customers that includes, but is not limited to: installation and service of diagnostic instrumentation, after-hours phone support, holiday and weekend on-site support, marketing, exhibitions, and clinical trials support.

Install and service instrumentation with minimum direct supervision, as requested, by the Service Center in accordance with current ISO (International Organization for Standardization) and GMP (Good Manufacturing Practices) standards. Provide follow-up service by calling customers who have recently been provided service. Ensure service was complete and satisfactory to the customers' needs. Properly maintain car stock inventory, test equipment, tools, and technical data. Complete service documentation, as required, by the position function or requested by System Support Engineering Manager in accordance with current GMP requirements. Display maturity and judgment in time management and expense control. Maintain expense levels within the established guidelines for field service travel and sites visits. Report quality control and other technical problems, in detail, to the Service Center and System Support Engineering Manager.Properly maintain and utilize company vehicle as outlined by current Corporate fleet policy.

Interface effectively with other departments and managers to resolve customer problems and issues.
Perform other duties as assigned. Accountable for providing support to customers that meet BD standards of
superior quality service at all times. Accountable for Company issued credit cards, travel advances, company
vehicle, trunk stock of spare, and repair parts. As a representative of BD, promote and maintain good customer
relations through high standards of personal appearance, ethical behavior, maturity and good judgment.

Qualifications

* Experience with medical devices and equipment, PC/software/LIS/networking/database management knowledge is highly desired.
* Requires a good working knowledge of electronics and electro-mechanical devices.
* Must have effective communication and customer service skills including technical writing and training.
* Must have effective interpersonal skills, organization/prioritization and administrative skills.
* Associate's Degree in Electronics/Computers/Biomedical Engineering is required.
* Minimum 4 years of recent relevant field service experience in servicing complex electronics also required.
* PC-based equipment and application software knowledge highly preferred.

Job
Technical / Field Service

Primary Location
US-California

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Field-Service-Engineer-Job-CA/619425/6194256194252010-04-10BDfull-timeUSDstarting0BSUS-California
About BD:
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The R&D Senior Scientist will initiate, lead, and execute cross functional and cross-divisional projects that support development and production of dehydrated culture media and components for cell culture and microbial fermentation. The successful incumbent will be able to assess and investigate the impact of media and media components on the cellular metabolic pathways and processes of both eukaryotic and non-eukaryotic cell systems. This position will also be responsible for formulation and generation of representative pilot samples for internal and external customer evaluations through the use of appropriate scale-down process models. Other duties include process optimization and product enhancement activities, as well as, internal and external communications, such as co-authoring or presenting posters or scientific presentations at international conferences.

The Senior Scientist works closely with R&D scientists, Procurement, Quality Engineers, Marketing, as well as, external and internal customers and vendors to define, design and implement solutions for product technical support needs and new product development.

Principal Accountabilities:

· Provide cell biology leadership for functional, cross-functional, and cross-divisional product activities

· Support Six Sigma tool applications

· Lead new product development and support activities

· Train associates on newly developed products or assays

· Co-author application notes, posters, presentations, and technical bulletins, for BD product development projects

· Maintain and grow bench skills and expert knowledge of current scientific literature, and state-of-the-art technologies, theories and principles in own area of scientific discipline

· Communicate technical information to both internal and external customers in a team environment

Qualifications

Qualifications:


· Expertise with cell metabolism, cell signaling and biochemical pathways are required

· Track-record of leading teams and project management experience is required

· Proficiency with microbiological and/or mammalian cell culture techniques and assays are required

· Research, Industrial or Clinical laboratory experience is required

· Knowledge of Design for Six Sigma or Six Sigma tools is preferred

· Experience working with powder media components, media formulation and media preparation, bench top or pilot scale is helpful

· Demonstrated excellent interpersonal skills

· Good communication skills (written and oral)

· Significant skills in mainstream computer software

Education and Experience Required:
BS degree with 7-10 years, MS degree with 5-8 years or PhD with 2 - 4 years of industry experience or equivalent required. Degree in Cell Biology, Biochemistry, Biotechnology, Microbiology or related science is required

Job
Other

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Senior-Scientist-Job-MD-21201/622826/6228266228262010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD is a global medical technology company that manufactures and sells medical devices, instrument systems and reagents, and is dedicated to enriching people's health throughout the world.

The company has its headquarters in scenic Franklin Lakes, NJ, close to major metropolitan routes that provide easy access to numerous academic, arts, leisure, sports and historic areas of interest.

BD offers a very competitive compensation and benefits package, strong leadership commitment to individual development and learning, and on-site fitness centers at our Franklin Lakes location.

To apply for a position, please log on to www.bd.com/careers/us, click on “Search Jobs” and follow the guidelines to locate your position of interest.

About us

Description

Reporting to the VP of R&D, this R&D Director will manage (directly and indirectly) a group of 10-20 engineers, scientists, and technicians who are responsible for on-time and on-budget delivery of product development milestones.

· Works with the R&D VP to develop and implement R&D strategies

· Makes and implements resource allocation decisions in support of prioritized portfolio objectives

· Oversees the development of R&D specific project plans that are created by R&D project Core Team Members (CTM's)

· Holds weekly reviews with CTM's to ensure that projects are on schedule and makes appropriate course corrections when needed

· Ensures functional excellence in R&D by:

o Helping project CTM's build appropriate risk management strategies into their project plans

o Conducts first-principles reviews with project CTM's to ensure soundness of technical approach early in project lifecycles

o Ensures that appropriate requirements planning is completed in conjunction with Marketing so that product development expenditures result in commercial successes

· Develops technology mapping and sourcing plans in support of key initiatives

· Drives key strategic technology initiatives

· In conjunction with IP council, builds and manages intellectual property strategy and plans

· Performs functional competency and capability assessments and develops and implements improvement plans

· Leads, manages and mentors his/her team and supports direct reports in the development planning and review process, including Talent Acquisition.

· Establishes and manages key technology partnerships (academics, consultants, inventors, industry).

· Establishes and manages OEM relationships.

· Develops and manages R&D budget. Works closely with CTL on project budgets.

· Acts as technical reviewer at DFSS and DFMA reviews and provides technical mentoring to R&D team members.

· Participates in VOC work to develop segment and product strategies.

Maintains relevant competency and compliance on product quality (PRP, Design History, DMS, QDMS).

Qualifications

BS degree in Mechanical Engineering, Materials Science, or Biomedical Engineering required, MS or Ph.D. a plus

Minimum of 7 years of progressively increasing responsibility managing R&D engineers in a fast-paced Medical or Diagnostic product development environment

Strong leadership skills

· Organization skills - The ability to distill objectives into a set of actionable activities.

· Decision making skills - The ability to organize a large amount of conflicting and

sometimes irrelevant information into a concise format. Willingness to make

tough/unpopular decisions when consensus does not exist within the team

· Functional expertise - 10 years in a Medical or Diagnostic R&D environment. Minimum of 7 years managing technical professionals

Project management skills

· Project management experience - Been involved in at least one successful or

unsuccessful project from beginning to end, where his/her input influenced the success or

failure of that project.

· Sense of urgency - An inherent sense of urgency or non-complacent personality.

· Project management software - Trained in the use of project management software.

· Project management concepts and theory - Trained on key project management concepts

such as critical path identification, proper definition and use of milestones, resource need

estimation and management, etc.

Strong interpersonal skills

· Mentoring ability - Recognize growth needs of individuals and willingness to council and

mentor members of the team to develop technical, organizational, and interpersonal

competency.

· Influencing skills - Build consensus on a plan of action among a team of individuals who

may have competing agendas. Ability to influence individuals who are not direct reports.

· Non-verbal communication awareness - Recognize, through non-verbal cues, when

individuals are: being pushed to hard, agreeing verbally but not mentally, overwhelmed,

afraid to offer an opinion, etc. The ability to extract input from all team members such that

their input is recognized and applied.

Presentation skills

· Speaking ability - Comfortable creating and communicating a compelling argument for a

course of action to a panel of senior executives and functional managers.

· Writing ability - Distill complicated information into an easily understood and compelling

case for a course of action.

Presence to interact with senior management

· Political astuteness - Awareness of organizational sensitivities/personal agendas and

ability to navigate through to garner support for a particular course of action.

· Confidence - Confidence that comes with professional experience and

having been involved in successful as well as unsuccessful projects.

Process orientation

· Strong process orientation - understands the value of process and its limitations.

· Familiarity with SCS process and Core Team structure and purpose.

Business skills

· Business case preparation and analysis.

· Familiarity with financial statements (P&L), Understanding of concepts such as Net

Present Value, Return on Investment, and other project financial metrics

Knowledge of Design for Six Sigma Methodology

Knowledge of Phase/Gate product development method

Job
Life Sciences R & D

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/R-26D-Director,-Preanalytical-Systems-Job/643875/6438756438752010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
Description

Responsible for improving process efficiency and product quality for reagent manufacturing. May be involved on cross functional teams within manufacturing or as part of New Product design transfer teams. Works on complex problems requiring an in-depth evaluation of various factors and root cause analysis. Exercises judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results. May determine methods and procedures on new assignments, and may provide guidance to other lower level personnel.

1. Analyzes and solves problems in Production and Quality Control.
2. Develops manufacturing methods and processes. Ensures new manufacturing processes can be scaled-up to produce products within specifications.
3. Evaluates technologies for reliability, reproduction capability, consistency, and cost effectiveness.
4. Develops validation protocols for manufacturing equipment and processes. Ensures validation of equipment and processes, evaluates data and writes reports.
5. Develops test methods and protocols.
6. Establishes and characterizes special test reagents and reference standards.
7. Reviews and signs off on QC data that fails QC tests. Evaluates failures, writes Variance Reports (VR's), presents recommendations to Material Review Board.
8. Evaluates product history, recommends revisions to product specifications, originates Change Orders (CO's).
9. Interfaces with Product Development, Research, and Production to bring new technologies, methods, and tests into Manufacturing.
10. Trains Chemists in new processes and procedures.
11. Keeps abreast of the basic requirements for compliance in own area of work and complies with those requirements. Participates as required in training on regulatory issues affecting own area of work. Brings regulatory compliance questions/issues to the attention of management.
12. Promotes a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices.

Qualifications

Qualifications:


* Requires a minimum of a Bachelor's degree.
* Requires a minimum of 8 years of hands on laboratory experience in a scientific research and development environment.
* A minimum of 1 year experience in a FDA or ISO regulated environment.

Assets:


* A MS or PhD
* Technical expertise in all major analytical techniques, instrumentation, and assays performed in reagent QC.
* Knowledge of GLP, GMP's and general laboratory safety.
* Knowledge of Regulatory requirements.
* Knowledge of methods for protein purification, conjugation to fluorochromes and haptens, immunochemical and immunoassay techniques highly desirable.
* Process transfer from Development to Manufacturing highly desirable.

Job
Manufacturing

Primary Location
US-California-San Jose

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-JOSE-Bioprocess-Engineer-II-Job-CA-95101/643878/6438786438782010-04-10BDfull-timeUSDstarting0BSSan Jose, CA, US
BD is a global medical technology company that manufactures and sells medical devices, instrument systems and reagents, and is dedicated to enriching people's health throughout the world.

The company has its headquarters in scenic Franklin Lakes, NJ, close to major metropolitan routes that provide easy access to numerous academic, arts, leisure, sports and historic areas of interest.

BD offers a very competitive compensation and benefits package, strong leadership commitment to individual development and learning, and on-site fitness centers at our Franklin Lakes location.

To apply for a position, please log on to www.bd.com/careers/us, click on “Search Jobs” and follow the guidelines to locate your position of interest.

About us

Description

The Pharmaceutical Systems (PS) R&D Senior Engineer will be a dedicated team member of a growing Platform. As a platform team member you will work in partnership with our Pharmaceutical customers on a cross functional product development team. Each platform team is responsible for designing and developing innovative Drug Delivery Systems that meet the specific and sensitive requirements of our Pharmaceutical customers and the needs of the patient.

The Senior Engineer is responsible for leading R&D activities from concept all the way through launch of the product including analyzing, prototyping, testing and validating the product The Senior Engineer may serve as either as a core team member or project team leader of cross functional product development teams including the manufacturing organization. As a project leader the Senior Engineer will maintain timelines and lead cross functional teams and deliver reports and updates to the larger organization

Main Responsibilities

* Manage multiple projects concurrently
* Translate customer, marketing, regulatory, medical and user requirements into specific, measurable functional product requirements
* Innovate and create novel solutions to complex technical problems
* Perform root cause analysis for field returns and production failures
* Understand and adhere to the Documentation process and design control elements
* Analyze and draw conclusions from test data for improving product performance
* Conduct design reviews, FMEA's and design verification programs
* Accountable/ responsible for successful and timely completion of designated tasks
* Utilize Design for Six Sigma (DFSS) Tools and Six Sigma methodologies
* Perform statistical analysis
* Ensure compliance with all local, state, federal, and BD safety regulations, policies, and procedures

Qualifications

Position Qualifications:


* BS Engineering, preferably mechanical or Biomedical and experience in product development. Advanced degree desired
* Minimum 5 years of experience in engineering preferably in the pharmaceutical and/or medical device industry.
* 1-3 years experience in Project Management.
*
Experience in FEA, CFD, modelization (1st principal)

*
Experience in CAD software (ProE, Autocad)

*
Experience in Plastic Part design and molding is desired

*
Six Sigma Green Belt certification is desired

*
Prior Knowledge Design for Manufacturing/Assembly (DFM) preferred

Job
Mechanical Engineering

Primary Location
US-New Jersey

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Senior-Engineer-R-26D-Project-Lead-Job/643891/6438916438912010-04-10BDfull-timeUSDstarting0BSNJ, US
Description

Reporting to the Vice President and Chief Intellectual Property Counsel, the individual in this position will be the lead IP attorney for BD's Cell Analysis business headquartered in San Jose, California. The individual in this position will be located at the business headquarters and will work with a team of BD Law Group associates at that location, closely partnering with a Senior Counsel on transactional and other matters and managing a Senior Patent Agent and a paralegal.

The position offers a high degree of autonomy and a unique opportunity to partner closely with business associates. We are seeking candidates with the ability to quickly understand the business' technology platforms and portfolio, to offer constructive and proactive input to business leadership to help shape business strategy, and to drive the tactical and transactional objectives required for strategy execution. The focus of the position will be on transactional matters, including IP license agreements, product evaluation agreements, R&D and other collaborative agreements and consulting agreements. There also will be extensive partnering with your peer Senior Counsel on more traditionally general transactional matters such as commercial supply and purchase agreements and mergers, acquisitions and divestitures.
.

Qualifications

The individual in this position will have an undergraduate, and preferably a post-graduate, degree in the life sciences, preferably cell biology. Bar admissions must include California and the United States Patent and Trademark Office.

Job
Patents / IP

Primary Location
US-California-San Jose

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-JOSE-Senior-Intellectual-Property-Counsel-Job-CA-95101/643898/6438986438982010-04-10BDfull-timeUSDstarting0BSSan Jose, CA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Senior Clinical Research Associate is a senior level position in the clinical monitoring developmental track. The Senior CRA's Experience and Knowledge will provide clinical trial monitoring and staff mentoring to support to the product development project. Performs Clinical Research Associate activities under the general guidance of the Director of Clinical Operations and Senior Clinical Trial Manager in compliance with BD Diagnostics - TriPath's Standard Operating Procedures, applicable regulations and guidelines, and industry standards. Monitors assigned clinical trial sites for compliance with the protocol and applicable regulations and guidelines. Participates in the development and implementation of clinical trial operations on assigned projects.

Principal Accountabilities:

1. Assumes the role of a general or project-specific Clinical Research Associate as assigned by the Senior Clinical Trial Manager. Performs clinical trial site management activities for assigned sites as required to ensure appropriate contact and management of sites. Ensures study site compliance with the protocol, applicable SOPs, regulations, and guidelines. The Senior CRA is also expected to remain knowledgeable about current evolving regulations and guidelines concerning diagnostic, medical device and clinical trials in general, and will continue to receive clinical study monitoring training, both formal and on-the-job.

2. Specifically, the Senior CRA:

* Monitors assigned study sites according to BD Diagnostics - TriPath Standard Operating Procedures (SOPs), project-specific monitoring plans, and industry standards.
* Prepares site visit reports, confirmation and follow-up letters, and other monitoring documentation as required per company SOPs, study-specific Monitor Plans and industry standards.
* Performs monitoring visits at external and internal clinical research sites and/or laboratory research sites, including pre-study, initiation, routine interim monitoring, close out visits, and over-sight visits.
* Monitors the sites for GCP compliance and compliance with the protocol and sponsor requirements including protocol adherence and adherence to site- and sponsor-specific SOPs.
* Reviews study subject data in the form of source documents and case report forms (CRFs) pertinent to the study, resolves data queries developed during the site monitoring process, and ensures investigational product accountability.
* Performs trial coordination activities and specialized clinical trial activities (e.g., contract management, Protocol Deviation reporting, Serious Adverse Event management) as requested by the Senior Clinical Trial Manager and per company SOPs, study-specific monitoring plans and industry standards.
* Assists with the tracking of patient enrollment data, monitoring visit data, CRF tracking, etc. as required to meet overall department and project goals and deadlines.
* Maintain study contact information, and assists in data management query resolution.
* Facilitates the timely distribution of adequate supplies, forms, equipment, study devices, etc. to assigned sites as required. Assists with the preparation and distribution of study materials to sites, CRAs, CRO personnel, etc., as required for the project.
* Understands assigned clinical protocols and all associated study materials. Is able to write business correspondence and working practices. Effectively presents information and responds to questions form internal personnel, Clinical Operations/Affairs project team members, and external vendor personnel, both in person and over the telephone.
* Effectively operationalize clinical trial protocols at the site level to ensure compliance with the protocol and all applicable regulations and guidelines.
* Manages workload to ensure that quality monitoring is provided on time and within budget.

3. Under the general guidance of the Senior Clinical Trial Manager, interacts with external partners, which could include Contract Research Organization (CRO) personnel, to ensure the timely and cost-effective conduct of high quality clinical trials. When applicable, oversees the monitoring of sites by CRO personnel and contract/permanent Clinical Research Associates (CRAs), maintaining direct communication with the assigned CRA and reviewing trip reports and other relevant correspondence/documentation, as required, to ensure the study sites' compliance with the protocol and applicable SOPs, regulations, and guidelines.

4. Management of external partners (assigned clinical and laboratory study sites) which may entail oversight of

assigned Clinical Research Associates which must be carried out in accordance with the organization's

policies and applicable laws, as directed by the Director of Clinical Operations or designee.

5. Assists the project team(s) and/or other members of the Clinical Operations Department in the development of plans, protocols, training and documentation for clinical research studies:

* Independently prepares/designs and/or reviews informed consent form templates, case report forms and instructions, site selection materials, procedural manuals, project newsletters, and other project-specific documents required for the conduct of clinical studies.
* Works with assigned team members to ensure Investigator Essential Regulatory Documents are reviewed appropriately for completeness and compliance with applicable regulations and policies; ensures appropriate follow-up for noted deficiencies. Assists with the maintenance of study files.
* Drafts internal and external memos, reports, documents, and correspondence to assist in the ongoing management and coordination of assigned clinical trials.
* Participates in project team communications with internal staff, CRO personnel, other CRAs, and vendor representatives as required.
* Assists in the data management, biostatistics, and report writing of trial data by ensuring the resolution of data queries, reviewing draft documents, tables, and listings, and summarizing clinical trial data, as requested.

6. Provides monitoring and trial management training and mentorship to existing Clinical Research Associates and new CRAs. Mentors junior CRAs during co-monitoring visits. Prepares training materials and delivers training sessions as required to support staff development activities.

7. Provides co-monitoring of CRAs as needed for troubleshooting, problem resolution, or support for existing monitoring. Provides back monitoring and/or auditing at sites for quality purposes in accordance with company SOPs, industry standards, GCP guidelines for data and regulatory documentation integrity.

8. Responsibilities may include input and feedback from interviewing, training contractors, planning, assigning

and directing work; and providing input on CRA performance evaluations.

9. The Senior CRA is expected to act as an expert resource regarding the Regulations and Guidances pertaining to Clinical Study execution and monitoring worldwide.

10. Makes travel arrangements which are consistent with the BD Diagnostics - TriPath Travel Policy and assigned project budget(s).

Job Dimensions:

Work Environment:

* This position will be based in Durham, NC and will require office hours at that location.
* While performing the duties of this job the employee is occasionally exposed to fumes or airborne particles and toxic or caustic chemicals and human or animal tissue. This noise level is the environment is quiet to moderate.

Accommodations:

* Reasonable accommodations may be made to enable individuals with disabilities to perform the ESSENTIAL FUNCTIONS.

Travel:

* Senior CRAs / CRAs are expected to travel 60-80% of the time.

Qualifications

Education and Experience Required:

* Minimum of a Bachelor's degree in Life Sciences or related field.
* 4 - 6 years of direct clinical trial monitoring experience
* Experience monitoring for the medical diagnostics industry
* Knowledge of lab diagnostic testing
* Previous experience leading or mentoring others
* Excellent interpersonal skills, including the ability to perform successfully in a highly matrix environment.
* High level of organization and ability to prioritize and handle multiple projects simultaneously.
* Knowledge of Good Clinical Practices and other regulations and guidances relative to the conduct and monitoring of clinical trials worldwide.
* Excellent written and oral communication skills, with the ability to articulate instructions
* Sound problem solving techniques, decision making processes, and ability to work efficiently and effectively with minimal supervision on routine work scopes.
* Proficient in Microsoft Word, Excel, PowerPoint, Lotus Notes, and Internet.
* Proven ability to interact effectively in a customer facing role.
* Excellent attention to detail.

Education and Experience Preferred:

* Graduate degree in life sciences or related field
* Experience with IVD (In Vitro Diagnostic) clinical trials strongly preferred
* Experience with laboratory monitoring
* Basic skills in electronic data capture applications
* Experience with trip report documentation and review
* ACRP and/or SoCRA certification

Job
Clinical Affairs

Primary Location
US-North Carolina-Durham

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/DURHAM-Senior-Clinical-Research-Associate-(IVD-strongly-preferred)-Job-NC-27701/643903/6439036439032010-04-10BDfull-timeUSDstarting0BSDurham, NC, US
Description

This position supports implementation of the strategic global Corporate Communications plan. It coordinates corporate and business messages to ensure consistency and alignment with global business objectives and corporate messaging. It also has responsibilities involving work on change management/organizational and transactional communications, crisis communications and site/facility communications for BD locations around the world. This position is a key overseer of quality of communications material globally, helping ensure consistency and conformity with corporate guidelines. Work with the Director, Corporate Communications and Manager, Internal Communications to support strategic global Corporate Communications plan deliverable. Serve as the primary liaison with the product Public Relations team to coordinate corporate and business messages to ensure consistency and alignment with global business objectives and corporate messaging. Assist with production of the Company's Annual Report and Sustainability Report. Work with various locations and departments to create or edit internal news items for global intranet; uses content management tool to post news articles and updates to intranet. Serve as a copyeditor to ensure adherence to corporate style and identity guidelines. for announcements, newsletters and other collateral originating from regional offices, Human Resources, Diversity/Inclusion, Social Investing, Marketing, etc. Enhance and maintain department's infrastructure for both internal and external purposes such as responses to media inquiries, presentations, surveys, awards programs, etc.
Additional responsibilities include:

Working on change management/organizational and transactional communications, crisis communications, and site/facility communications for locations around the world.
Working closely with senior management as well as departments including Investor Relations, Government Relations, Regulatory Affairs and Finance.

Qualifications

REQUIRED

Minimum of 5 years of progressively responsible communications experience, including some time at a public company.

· Media relations experience, including pitching stories to national media outlets.

· Proven writing capabilities in a variety of formats, including executive speeches, press releases and other collateral materials, employee newsletters, organizational communications, video scripts and PowerPoint presentations.

· Ability to prioritize and multi-task in a fast-paced environment.

· Excellent interpersonal and verbal communications skills, in addition to written skills

· Advanced editing and proofreading skills, along with extraordinary attention to detail.
Strategic thinking and planning skills.

· Experience working globally/cross-culturally.

Flexibility/adaptability.

Bachelors Degree; Advanced Degree preferred.

PREFERRED

· Communications experience in medical technology or healthcare.

· Familiarity with social media tools and fundamental graphic design skills.

RESUMES SUBMITTED WITHOUT "COVER LETTERS" WILL NOT BE CONSIDERED.

Job
Communications / Promotion

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Manager,-Corporate-Communications-Job-NJ-07417/643904/6439046439042010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

We currently have an opportunity for an intern to work in our Engineering Department at our Broken Bow, NE Facility . The intern will be working with the direction of the Engineering Supervision. The intern will assist in engineering projects through mechanical engineering and project management. The intern will have the development opportunity to gain vast knowledge and experience in Mechanical Engineering.

Assignments may be summer or semester based.

Qualifications

* A graduating high school senior enrolling or a student currently enrolled in accredited college or university.
*
Previous academic and/or work related experience/skills in Mechanical Engineering preferred.

*
Seeking candidate with basic electrical and mechanical knowledge along with troubleshooting skills.

*
Excellent analytical skills

* Outstanding communication skills and ability to work across functional boundaries
* Preference given to dependant of a BD associate, however external college students will be considered.

Prior internships in related fields preferred but not required.

Physical Requirements

Medium work: Exerting up to 50 pounds of force occasionally, and/or up to 25 pounds of force frequently, and/or 10 pounds of force constantly to move objects.

Job
Mechanical Engineering

Primary Location
US-Nebraska-Broken Bow

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BROKEN-BOW-Intern-Engineering-Process-Electrical-Job-NE-68822/643911/6439116439112010-04-10BDfull-timeUSDstarting0BSBroken Bow, NE, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The R&D Scientist will execute cross functional and cross-divisional projects that support development and production of dehydrated culture media and components for cell culture and microbial fermentation. The successful incumbent will apply scientific principles to the performance of laboratory tests associated with the research and development of media formulations, specifically at the bench top bioreactor level through setup, operation, and maintenance of various bioreactor systems. Other duties include process optimization and product enhancement activities, as well as, internal and external communications, such as co-authoring or presenting posters or scientific presentations at international conferences.

The R&D Scientist works closely with R&D leadership, Procurement, Quality Engineers, Marketing, as well as, external and internal customers and vendors to implement solutions for product technical support needs and new product development.

Principal Accountabilities:

· Provide bench scale bioreactor/fermentation excellence for functional, cross-functional, and cross-divisional product activities

· Support Six Sigma tool applications

· Execute new product development and support activities

· Train associates on newly developed products or assays

· Co-author application notes, posters, presentations, and technical bulletins, for BD product development projects

· Maintain and grow bench skills and expert knowledge of current scientific literature, and state-of-the-art technologies, theories and principles in own area of scientific discipline

· Communicate technical information to both internal and external customers in a team environment

Qualifications

Education and Experience Required:
BS degree with 3-5 years, MS degree with 2-3 years or PhD with 1-2 years of industry experience or equivalent required. Degree in Cell Biology, Biochemistry, Biotechnology, Microbiology or related science is required. Experience running bioreactors is a must.

Qualifications:


· Expertise in mammalian and microbial fermentation at bench top scale with multiple types of systems/formats

· Demonstrated knowledge of equipment/system setup, operation, and maintenance

· Proficiency with microbiological and/or mammalian cell culture techniques and assays are required

· Research, Industrial or Clinical laboratory experience is required

· Knowledge of Design for Six Sigma or Six Sigma tools is preferred

· Demonstrated excellent interpersonal skills

· Good communication skills (written and oral)

· Significant skills in mainstream computer software

Job
Product Design / Development

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Scientist-Job-MD-21201/643925/6439256439252010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Under the direction of the Sr. Complaint Coordinator, assumes responsibility for the effective functioning of the complaint handling system database and complaint investigation, including direct responsibility for the work of customer contact interface, and preparation of Quality Trends report and other reports as requested. Provides support in the development, maintenance, and improvement of hardware/software support tools for complaint handling. Provides strong/general computer hardware/software support to the department and provides support inside and outside department with computer productivity tools.

1. Provides inputs to the customer complaint-handling system. Ensures timely handling of investigation complaints.

2. Maintains a high level expertise in area of regulations regarding complaint handling. Acts as an informational resource for the organization.

3. Maintains computerized complaint tracking system related to product incidents and product liability. Continually evaluates system and identifies and implements

improvements in methods and tools to manage it more efficiently.

4. Perform complaint investigations, when required.

5. Ensures quality of complaint handling output through final signoff authority and master file maintenance.

6. Promotes quality awareness and effective communication to develop, maintain and improve the effectiveness of the quality management system. Through

education and consistent application of sound quality assurance principles, assure that the Company products, processes and services satisfy customer and

management requirements.

7. Assists in the maintenance of the database for the Quality Trends Report (monthly).

8. Uses computer expertise in maintaining all QA/RA hardware and software and develops and implements productivity tools for the department. Provides similar

support outside department as time permits.

9. Complies with all local, state, federal, regulations and with all BD safety, quality, and general policies, procedures, and practices.

10. Provides support service for Becton Dickinson legal in response to litigation as requested.

(a) Respond to product liability claims.

(b) Investigate-identify product-perusal hospital records and other discovery materials.

(c) Aid legal counsel as applicable.

(d) Answer interrogatories and produce documents and other production, as required.

(e) Coordinate the availability of appropriate expert witnesses for depositions and trials.

(f) Appear, as needed, at depositions and/or as a corporate representative at trial.

11. Complies with all local BD quality polices/procedures/practices through consistent application of sound Quality Assurance principles.

12. Other tasks, as assigned.

Qualifications

EDUCATION: Minimum education required to perform duties.

Bachelor's Degree or five years of Medical Industry experience with

two of those years in complaint handling.

EXPERIENCE: Minimum years required, both inside and outside company, to perform duties.

Five years in Medical Device Industry with knowledge in the areas of Quality Assurance, FDA Regulations, QSR's,

and Laboratory functions.

Effective communication and people skills.

Excellent technical writing skills.

Proficient in Microsoft Office.

SAP experience desirable.

Job
Regulatory Compliance

Primary Location
US-Utah-Sandy

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SANDY-Regulatory-Compliance-Complaint-Analyst-Job-UT-84070/643935/6439356439352010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
Description

The Marketing Manager has responsibility for a broad strategic group of Research products for core Academic and Pharmaceutical market use. Working closely with the Marketing Director, aids in the development, and on-going evaluation, of the annual product portfolio. The Marketing Manager is expected to assist in strategic planning efforts, as well as, cultivate effective working relationships with R&D, Business Development, Sales, Operations and Finance. Accountable for marketing management activities required to implement and administer division and corporate objectives. Develops and maintains product marketing plans to produce maximum sales, growth and profitability. Establishes and maintains a strong competitive position through promotional and communication programs. Is responsible for product line P&L, and should be highly adept at financial analysis and business case preparation. Conducts appropriate market analysis and competitive product research to provide information on market segmentation, market share, customer perceptions and future North American and international market trends. Directly supervises 1-2 marketing professionals. Assumes training leadership role in establishing general product management fundamentals. Establishes, implements and maintains "best practices" in product management. This position requires 30% travel (domestic and international).

Qualifications

Qualifications:


*
A minimum of a Bachelor's degree

*
A minimum of 3 years experience with Flow Cytometry.

*
A minimum of 7 years life science product marketing experience.

*
A minimum of 2 years of management experience.

*
Ability to travel a minimum of 30%.

*
Mastery of Excel and PowerPoint required.

Assets:


*
Demonstrated ability to manage all aspects of product marketing plans to ensure the achievement of financial expectations and product line strategies.

*
The selected candidate should demonstrate effective analytical, problem solving, organization and prioritization skills, with a special attention to detail while maintaining overall perspectives.

*
Ability to develop comprehensive business cases with detailed financial analysis.

*
Results oriented, capable of managing and driving the completion of multiple competing projects.

*
Demonstrated ability to manage all aspects of product marketing plans to ensure the achievement of financial expectations and product line strategies.

*
Excellent written, oral, and interpersonal skills are expected.

*
Must have effective meeting management skills.

*
Experience presenting to senior level management.

*
Prior experience with stage-gate product development preferred.

Job
Strategic Marketing / Planning

Primary Location
US-California-San Diego

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/SAN-DIEGO-Marketing-Manager-Job-CA-92101/643940/6439406439402010-04-10BDfull-timeUSDstarting0BSSan Diego, CA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Acute Care Sales Consultant is responsible for selling the Medical Surgical Systems' product portfolio to the US acute care healthcare market segment. The portfolio includes Injection, Infusion, Surgical Blade, Scalpel, and Anesthesia product lines. The customer base is comprised of US hospitals that are 100 beds in size and larger (including facilities on hospital grounds and those that are owned by the hospital).

The Acute Care Sales Consultant manages his/her territory according to a FOCUS Account strategy, calling on the 20-25 hospitals that represent 80% of the territory's current volume and ADC beds. Selling tactics include deep account penetration, broadening of departmental relationships, system selling, and use of marketing tools to communicate clinical and economic value.

Primary responsibilities include: (1) Meeting/exceeding sales budget for assigned territory; (2) managing incremental conversion opportunities from initial targeting, through evaluation, product ordering, and inservicing; (3) maintaining existing business; (4) implementing Marketing initiatives; (5) implementing national/regional contractual agreements; (6) providing routine performance reporting; (7) working collaboratively with members of MSS Regional team and across BD units with other BD field associates; (8) working with local distributor branches servicing the territory; (9) utilizing available sales support resources; and (10) exemplifying the BD core values

This position covers the Richmond, VA area.

Qualifications

Required Skills: Sales proficiency, computer proficiency (Word, Excel, PowerPoint), territory and account management

Required Degrees: Bachelors Degree

Years of relevant work experience: a minimum of 3 years of sales experience is required

Job
Field Sales

Primary Location
US-Virginia

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Field-Sales-Consultant-Acute-Care-Richmond,-VA-Job-VA/648444/6484446484442010-04-10BDfull-timeUSDstarting0BSUS-Virginia
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The Primary Care Sales Consultant is responsible for selling the Medical Surgical Systems' product portfolio to the US alternate site healthcare market segment. The portfolio includes Injection, Infusion, Surgical Blade, Scalpel, and Anesthesia product lines. The customer base is comprised of various alternate sites and US hospitals that are below 100 beds in size. The alternate sites include independent ambulatory surgery centers, large specialty clinics, pain management centers, public health departments, primary care physicians, long-term care, and academia.

The Alternate Site Sales Consultant manages his/her territory according to a FOCUS Account strategy, calling on the top 50 accounts according to existing business and revenue potential. An extended customer reach is achieved through collaboration with Distributor Sales Representatives, the Telesales function, and other forums

Primary responsibilities include: (1) Meeting/exceeding sales budget for assigned territory; (2) managing incremental conversion opportunities from initial targeting, through evaluation, product ordering, and inservicing; (3) maintaining existing business; (4) implementing Marketing initiatives; (5) implementing national/regional contractual agreements; (6) providing routine performance reporting; (7) working collaboratively with members of MSS Regional team and across BD units with other BD field associates; (8) working with local distributor branches servicing the territory; (9) utilizing available sales support resources; and (10) exemplifying the BD core values

Qualifications

*

Required Skills: Sales proficiency, territory and account management

*

Required Degrees: Bachelors Degree

*

Years of relevant work experience: minimum of one (1) year of experience is required

*

Excellent communication, interpersonal and analytical skills a must.

*

Must have a demonstrated successful sales track record, solid negotiation skills, understanding of buyer/decision maker types, exhibit effective selling, listening, and verbal/presentation skills, and ability to assess and respond to customer needs.

* Intermediate proficiency in Microsoft Word, Excel and PowerPoint required.
* Former clinical experience preferred.
* Must have demonstrated experience in managing both internal and external budgets and resources, conducting pre-call planning, and ability to prioritize and segment accounts.
* Must be willing to travel 25%

Job
Sales Representative / Account Management

Primary Location
US-California

Shift
Rotating

Relocation Available
No]]>http://www.bd-careers.com/job/Field-Sales-Consultant-Primary-Care-Orange-County-Job-CA/648449/6484496484492010-04-10BDfull-timeUSDstarting0BSUS-California
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

This position is in the Canaan CT facility located in the Northwest Corner of CT 2 hours from NYC and 21/2 hours from Boston.

About us

Description

Process Engineer - Molding

This position is accountable for the development and execution of strategies for optimizing mold equipment usage, operation and efficiency in a High Volume injection molding production environment. The position will provide daily Process Engineering support to production by troubleshooting problems and providing direction to technical personnel to resolve issues.

This position will be part of the High Volume Business Leadership Team and also lead the Mold Technology Group to provide support and direction for all molding processes within the Canaan Facility. Work with Plant Quality, Molding Team Members, Molding Technical Associates and vendors to achieve business goals.

Responsible for:

* Leadership and direction of the Mold Technology Group
* Achieving mold and press productivity, waste reduction and uptime goals
* Directing the maintenance of existing assets and installation of new equipment
* Interfacing with the Toolroom to ensure Preventative Maintenance is completed on time without impact to production as well as assisting with any Breakdown maintenance that occurs.
* Making technical decisions with input from Operations and Engineering Managers
* Development and execution of Cost Improvement Projects from Budget Proposal through execution
* Providing project management for new equipment installation, validation and release to production
* Collaboration with cross-functional teams to complete assigned projects and drive improvement
* Coordination and communication of project status to applicable department and plant leadership
* Interfacing with molding production associates to provide direction, improve control plans, transfer new molds and/or processes

Qualifications

Minimum Education: B.S. degree in Mechanical Engineering (Plastics Engineering preferred)

Minimum Experience: A minimum of 5 years of engineering experience in a High Volume production environment, preferably with emphasis on Injection Molding. Strong diagnostic, troubleshooting and project management skills. Leadership experience (direct reports or team based) desired. In depth understanding of mold flow, plasticizing, and theory desired. Proficient computer skills (Microsoft Office/CAD packages). Working knowledge of Six Sigma (Greenbelt/Blackbelt desired) and Continuous Improvement / Lean preferred.

Job
Manufacturing

Primary Location
US-Connecticut-Canaan

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/CANAAN-Process-Engineer-Molding-Job-CT-06018/649646/6496466496462010-04-10BDfull-timeUSDstarting0BSCanaan, CT, US
BD Biosciences, a segment of BD, is one of the world's leading businesses focused on bringing innovative research and clinical tools to life scientists and clinicians. Principal product lines include fluorescence activated cell sorters and analyzers; cell imaging systems; monoclonal antibodies and kits; research reagent systems; tools to aid in drug discovery and growing tissue and cells; and diagnostic assays. Its customers are involved in basic research, the discovery and development of drugs and vaccines, clinical trials, diagnostic testing and disease management. This diverse customer base includes academic and government institutions, pharmaceutical and biotech companies, and clinical laboratories.

BD Biosciences is an Equal Opportunity/Affirmative Action Employer

About us

Description

BD Biosciences is currently seeking enthusiastic Software Engineers to join our exciting and growing team. At BD Biosciences you will have the opportunity to create Systems that are used to help all people live healthy lives. So why wait? Apply today!

The Software Project Engineer will be responsible for providing a technical leadership by researching, recommending, estimating, prototyping, and/or initiating the development of products, methodologies, and technologies. Additional responsibilities will include creating new software component designs and enhancements to existing software products. Demonstrated experience in the design and implementation of complex windows desktop applications a must. Overall experience will include modeling & design with tools such as Rational Rose, UI design & development. Experience in good software engineering practices and methodologies are a must. The Ideal candidate will have prior experience in architecting and building complex windows applications with a keen sense of usability.

Qualifications

Qualifications:


* A minimum of a Bachelor's degree.
* A minimum of 4 years of software development experience in Java.
* A minimum of 6 years of experience using Object Oriented Design.
* A minimum of 6 years of experience using Object Oriented Programming.

Assets:


* Individuals with a Computer Science or related engineering or scientific degree are desired.
* Experience in Swing framework in Java
* Working with off shore/ Remote teams
* Experience in Software Project Management

Job
Software Engineering

Primary Location
US-California-San Jose

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-JOSE-Software-Project-Engineer-Job-CA-95101/651769/6517696517692010-04-10BDfull-timeUSDstarting0BSSan Jose, CA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

With limited direction from the Manager of Manufacturing Support, the Molding Technology Engineer is responsible for developing and supporting the Molding and Molding Process within Diabetes Care to:

· Lead Diabetes Care Molding activities to support the new product development projects as they relate to molding and molded part design, particularly injection molding.

· Evaluate and provide input into product component design, moldability analysis (FEA, MoldFlow, etc), tool construction, press configuration, vendor selection, validation strategy, standardization, technology assessment / implementation and process optimization.

· Providing support to meet project deadlines and milestones by interfacing with the R&D, QA, Operations and Manufacturing both within Diabetes Care, BDX and external suppliers / vendors.

· Plan, design and coordinate the development and implementation of plastic molding processes and related quality/engineering activities to support new product development activities.

· Also provide technical support to molding operations and support trouble-shooting with existing molds or continuous improvement efforts.

· Lead new process development activities related to molds and tooling, as well as changes to the existing molds if applicable. Includes assessing and determining needs; such as: shrinkage, draft angles, tolerances, material needs, etc.

· Specify equipment, tooling and fixtures for new processes, or existing process changes. Oversee project to install or change mold related equipment as assigned by manager.

· Coordinate and carry out qualification and validation activities for new products, processes, changes and transfers as required.

· Coordinate and communicate assigned projects and their status with the appropriate personnel and departments.

· Incumbent executes responsibilities with a large degree of autonomy requiring minimal day-to-day oversight by immediate supervisor.

· Incumbent must engage and gain the support of associates in various positions of responsibility and in various functions within BD worldwide.

· Incumbent represents BD when interfacing with external vendors / suppliers as processes are developed and capital equipment is purchased.

· All activities are conducted in compliance with applicable standards and regulations.

Qualifications

· B.S. Degree in mechanical, manufacturing or mold engineering or a related science field.

· Tool and Die Maker training desirable.

· Training in design of experiments and statistics including Six Sigma methodology desired.

· Five to Ten years of experience working in a high volume molding environment including design, qualification, validation and building molds.

· Experienced in Project management in the design / development of molding equipment and related processes. Experience in the area of Medical sterile disposable devices is preferable.

· Effective communications skills are essential. Experience in working with equipment suppliers and all levels of manufacturing plant personnel.

· Knowledge of the interrelationship of Manufacturing Operations and Finance, Quality, Regulatory and Supply Chain in an FDA/ISO regulated environment. Experience in interfacing with these functions to achieve objectives.

· Experience in preparing equipment specifications, capital appropriations and process validation documentation.

Job
Manufacturing

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Molding-Technology-Engineer-Job-NJ-07417/652510/6525106525102010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Core Team Leader leads the cross-functional Core Team and Extended Team in executing all aspects of product development projects including successful product development over the complete product life cycle (inception through development, high volume manufacturing, post launch and commercialization). The Core Team Leader is ultimately responsible for the execution, quality and results of his or her project and the success of the resulting product in the market. The Core Team Leader is responsible for the creation of the project work breakdown structures, integrated business plans and product requirements. He/She manages day-to-day activities of team members, tracks progress against plan, manages the project budget, identifies project risks and provides plans to mitigate those risks. The Core Team Leader should be capable of managing varying degrees of program and project size, cost, complexity or risk.

The Core Team Leader is responsible and accountable to lead and direct cross-functional activities and outcomes including:

· Planning resource requirements and negotiating team resource assignments with functional managers

· Leading the creation of the cross-functional project plan, including budget and resource planning, to fulfill the product concept.

· Aligning and managing all cross-functional activities to deliver the product on time and on budget per contract while meeting all agreed upon technical, operational, business and customer requirements.

· Negotiate, resolve personal/team conflicts and project/functional conflicts., and drive consensus among team members to accomplish project and business goals

· Defining, refining, and understanding customer requirements.

· Successfully track progress to requirements, plan and resolve deviations

· Architecting or refining the high-level product concept to fulfill the customer requirements.

· Providing work definition and direction to the assigned cross-functional Core Team Members.

· Providing coaching and mentoring to Core Team members and providing significant feedback to functional leaders regarding training needs of, and resources required by, the core team.

· Providing meaningful and significant input to the performance of core team members that is fully considered in their year-end performance reviews and compensation recommendations.

· Successful commercial, design, and business project reviews; makes PDT aware of, and proposes solutions to, unanticipated or potential issues/concerns as soon as they are known.

· Successful product design.

· Superior product quality in the field.

· Product acceptability by intended customers; spends time with customers/end-users and constantly invests in understanding customer environment.

· Successful product commercialization.

· Completion of accurate and timely reporting, e.g. project portfolio server (G3), resource allocation, dashboard updates.

· Contributes to the continuous improvement in organization's ability to execute programs and projects from initiation through launch.

· Coaching and mentoring new Core Team Leaders.

Qualifications

* BS in Engineering required, preferably mechanical, chemical or biomedical.
* Masters required preferably in mechanical, chemical or biomedical engineering. MBA or PhD preferred.
* 8 + years successful project & program management experience with new and complex medical devices
* PMI training preferred
* Has successful launched multiple new medical device products from concept through launch
* 8 to 15 years medical device product development and high volume manufacturing experience
* Experience with drug/device combination products & medical device clinical trials
* Experience with biological medical fluids and polymers a plus
* Must be a skilled and determined communicator and negotiator
* Must have strong leadership skills and be very relationship and collaborative oriented

Knowledge of specific procedures/practices

* Product Development Phase gate Processes and Procedures
* Quality System Regulations for Medical Devices
* Technology Development Process
* Product Development Performance Metrics
* Preliminary and Integrated Business Plans
* DFSS/DFMA
* Post Launch Reviews
* Voice of Customer Methodologies
* Team Formation and Dynamics
* Project Management

Job
Product Design / Development

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/Core-Team-Leader-R-26D-Infusion-Platform-Job/652514/6525146525142010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

As part of the Worldwide Marketing Team, the Senior Marketing Manager - Multiplexed Assay Products will manage the market assessment, market and product development and planning activities and strategies for BD Diagnostics - TriPath's Multiplex Cancer Diagnostic product line including current product development efforts, development of a platform/product line roadmap, future product introductions, product improvements, and life cycle management. Through the management and support of a team of Marketing professionals, the Sr. Marketing Manager - Multiplexed Assay Products provides leadership and action to drive and ensure implementation all marketing efforts through the development and execution of marketing strategies, objectives, plans, and accompanying budgets for this product line. This may include serving as a Marketing representative on product development teams and being responsible for completing respective Marketing deliverables of GPDS.

Principal Accountabilities:

1. Through voice of customer, market analytics, competitive assessment, and other quantitative analysis, develops and execute worldwide objectives, strategies, and plans for new products and product lines in the multiplex cancer diagnostic portfolio including product features, pricing strategies, and competitive advantage plans.
2. Working with the VP Marketing and other Team members develops and communicates the product line roadmap for the multiplex oncology platform including desired menu content, instrument, software, and automation solutions.
3. Supports the Global Product Development System (GPDS) process as a core team member (CTM) and/or leader of CTMs. GPDS responsibilities are focused on inbound activities predominately associated with the concept and design phases. Helps ensure GPDS functional excellence.
4. In conjunction with the various worldwide teams, ensures the approved strategy is executed across all customer segments and geographies.
5. Manages one or more Marketing and/or Product Managers and appropriate support personnel responsible for multiplex cancer diagnostic related products to develop and implement customer-driven market activities.
6. Participates on core teams with multi-functional/multi-divisional involvement responsible for multiplex cancer diagnostic products and/or related products and is accountable for completion of respective Marketing deliverables, if assigned. Includes driving market-related initiatives through communications and collaborative efforts with all levels of other functional areas represented on project teams (e.g. R&D, Regulatory Affairs, Quality Assurance, Legal, Finance, etc.).
7. Works in close conjunction with other Marketing group leaders (Commercial Marketing, International Marketing, and Marketing/Business Development) to gain input on worldwide product/portfolio plans from respective regions and to develop and implement global cross product support capabilities for the assigned product line.
8. Working with BD Diagnostics - TriPath's Chief Scientific Office and/or Medical Directors, help identify and develop relationships with key opinion leaders (KOLs), key customers, professional associations/societies, and patient advocacy groups to develop advocates, refine product requirements and educate industry leaders on BD Diagnostics - TriPath's multiplex cancer diagnostic products.
9. Develops and manages marketing expense budgets for multiplex cancer diagnostic programs to support approved/assigned strategy and tactics.
10. Develop worldwide revenue forecasts for new products, and once commercialized, work with Sales Management to develop a system for, measuring and positively affecting product related metrics such as sales volume, average selling price and market share.
11. Undertakes various marketing activities, e.g. attendance at scientific meetings, customer visits, regional market meetings, marketing research, etc. to stay current on issues related to customer needs as well as future market opportunities.

Job Dimensions:

* Manage multiplex cancer diagnostic product portfolio metrics including Marketing deliverables for BD Diagnostics - TriPath's product development system, major Marketing development milestones, and commercial excellence progress including working with respective Core Team Leaders, extended team members, and other functional areas to develop worldwide launch and continuing commercialization strategies.
* Provide ongoing recommendations to core team on product modification, cost reduction, margin analysis, clinical trial design and regulatory strategy.
* When appropriate (post launch) manage multiplexed assay product metrics such as sales volume, revenue, average selling price, etc.
* Manage the associated Marketing expenses and operating budgets.
* Management of a group of people no less than 1.
* Travel required, ~20%.

Qualifications

Education and Experience Required:

* Bachelors Degree in Marketing, Management, Communications, Business Administration or technical related field.
* Minimum of 7-10 years in marketing management, including a focus in product management.
* Experience with development and launch of medical systems and instruments, preferable cancer diagnostic related, into worldwide clinical lab segments including high volume core labs, immunoassay, chemistry, or molecular testing areas.
* Knowledge of the sales process for placing complex IVD equipment in clinical laboratories.
* Experience in reimbursement and pricing strategies for introduction of new medical products in the US market, including development of medical economics models and economic publications.
* Demonstrated leadership and track record of achieving results through the development and execution of marketing strategies and plans.
* Demonstrated experience in diverse team environment, including coordination, problem solving, conflict resolution and consensus building skills.
* Experience in developing new products, preferably IVDs, from concept to launch through a Stage-Gated or similar system.
* Practical knowledge and experience in defining unmet customer needs and translation into product requirements.
* Experience managing third-party relationships and collaborations.
* Ability to demonstrate strong leadership skills and "lead by example" characteristics.
* Highly motivated self-starter that exhibits a high degree of professionalism at all times and possesses the highest moral and ethical standards.
* Demonstrated experience in managing multiple tasks in a compressed time frame. Utilization of project management software desirable.
* Excelling interpersonal, oral, written and platform communication skills. Individual must possess exceptional communication skills as well as the ability to interface across all functional areas.
* Proficient in MicroSoft® Office Suite products (Word, Excel, PowerPoint).

Education and Experience Preferred:

* MBA preferred.
* Experience with the development of marketing communications/channels for the reagent, software and instrument products, programs, and solutions.
* Previous experience in sales of IVD equipment in clinical laboratories.
* Firm understanding of laboratory workflow in clinical chemistry, immunoassay, or similar areas of clinical laboratories and impact of technology on workflow, efficiency, productivity and cost.
* Experience working with cancer disease detection and management, payers, and regulatory agencies (FDA and/or similar ex-us agencies).
* Experience working in the in vitro diagnostics (IVD) industry.
* Experience working in clinical immunoassay laboratory segments.

Supervisory Responsibility:

Manages one or more of the following positions: Associate Marketing Manager, Marketing Manager, Associate Product Manager, Platforms, and other Product Manager positions assigned by the Vice President of Marketing.

Job
Strategic Marketing / Planning

Primary Location
US-North Carolina-Durham

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/DURHAM-Senior-Marketing-Manager-Multiplexed-Assay-Products-Job-NC-27701/652517/6525176525172010-04-10BDfull-timeUSDstarting0BSDurham, NC, US
Description

Plans, designs and coordinates the development and implementation of processes related to support Cannula Operations world wide.

Develops cannula processing technology to maintain an industry leading position across the cannula operation sites.

Provides technical support to the R&D cannula development teams for the implementation of new products and be able to effectively communicate to all levels of management.

Provides technical support for Cannula production, and support trouble-shooting or continuous improvement efforts.

The skill sets required for completing projects are concepting of cannula processing automated equipment, implementing into production per project timeline and capital budget, documenting of operations, training and starting of production operations with in a team environment.

Responsibilities

1. Coordinate and carry out qualification and validation activities for new improved, processes, changes and transfers as required.
2. Focus on specific technical projects in cannula manufacturing technology or other engineering disciplines assigned by the Manager.
3. Coordinate and communicate assigned projects and their status with the appropriate personnel and departments.
4. Specify equipment, tooling and fixtures for new processes, or existing process changes.
5. Write capital expenditure requests for equipment, tooling and fixtures, as needed.
6. Install new equipment, tooling and fixtures to support new product development. Responsible for documentation and training.
7. Develop and implement processes for pilot production and scale-up programs.
8. Lead Projects as assigned.
9. In own field of scientific/engineering competence, maintain up-to-date familiarity with developments through attendance at professional meetings, literature and consultations.
10. Comply with all local, state, federal, and BD safety regulations, policies, procedures.
11. Comply with all local BD quality policies, procedures, and practices through consistent application of sound quality assurance principles.

SUPERVISION:

Potential for direct and indirect supervision in addition to the functional supervision and responsibility for all assigned projects.

ACCOUNTABILITY: All work is subject to review by the PAD Manager, Cannula operations Managers on a regular basis or at the conclusion of assigned projects.

Qualifications

EDUCATION:

B.S. Degree in mechanical, manufacturing or a related science field.

EXPERIENCE:

Ten (10) years of experience in various engineering fields relating to manufacturing, process development, automation and equipment design. Seeking experienced person in grinding operations and fixturing.

Job
Mechanical Engineering

Primary Location
US-Nebraska-Columbus

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/COLUMBUS-Process-Automation-and-Development-Engineer-Cannula-Operations-Job-NE-68601/655730/6557306557302010-04-10BDfull-timeUSDstarting0BSColumbus, NE, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

We are looking for an exceptional Principal Engineer to join our R&D team. Working in an R&D team, the Principal Engineer will lead the design efforts for product development projects in BD Medical-Diabetes Care. The ideal candidate will be experienced in designing and developing disposable medical devices for high volume manufacturing. This person will be a key problem solver and a potential core team leader to plan and lead cross-functional product development projects, from concept to manufacturing. This is a rare opportunity for a truly motivated individual to participate in the development of several new products related to the treatment of people with diabetes. The ideal candidate will have a logical approach to the solution of problems and to the product development process with the capacity for original thinking. Candidates should be prepared to present previous product development work during the interview process to demonstrate their abilities and experience.

Innovate and define technical solutions for design problems and lead efforts to realize the technical solutions.

Design, prototyping and testing of designs for new products

Perform 3D modeling and tolerance analysis

Design for Manufacturing/Assembly (DFM)

Uses engineering first principals and advanced engineering methods to guide the development process

Design fixtures for assembly, testing and inspection

Proactively interact with customers and health care providers. Comprehend and interpret their needs and requirements correctly and transfer the comprehension into novel product designs effectively

Conduct and participate in design reviews, DFMEA's

Write, implement and lead design verification protocols and activities.

Lead R&D functional planning, coordination and reviews for all phases of medical device development including concept development, detailed engineering and design for manufacturability.

Improve and incorporate novel features into existing products. Confirm product capabilities by designing feasibility and testing methods and systems

Qualifications

* BS in Mechanical Engineering required. MS in Mechanical or Biomedical Engineering or PhD Preferred
* Minimum of 8-10 years experience as a mechanical designer/ engineer in medical device industry.
* Experience in Diabetes Care systems and/or medical devices disposables
* Proficient in Pro/E and/or SolidWorks and GD&T
* Advanced knowledge of engineering first principals
* Experience developing and prototyping designs for technical & customer evaluations
* Ability to create novel designs based on Voice of Customer/customer needs
* Strong creative ability and advanced technical judgment
* Strong project management, prioritizing and multi-tasking skills to work within tight deadlines
* Strong analytical and problem solving skills, as well as a good background in product development process
* Demonstrated ability to effectively and clearly communicate concepts, ideas and knowledge to other individuals and teams
* Experience with ISO requirements and GMP guidelines, FDA regulations, medical device design control, and manufacturing scale-up processes a plus
* Excellent oral and written communication skills. Clear/Concise documentation and correspondence during project execution
* Previous fast career track a strong advantage

Job
Product Design / Development

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/Principal-Engineer-R-26D-Infusion-Platform-Job/655732/6557326557322010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
Description

General Function

Responsible for product management activities required to implement and administer Business and Unit objectives for assigned product line(s). Develops and maintains product marketing plans to exceed unit, revenue and profitability goals for assigned product line(s). Establishes and maintains a leading competitive position through strategic and identification and tactical implementation of marketing opportunities. Develops promotional and communication programs. Facilitates regional introduction of product launches and develops and administers revenue budgets and schedules. Establishes, implements and maintains "best practices" in product management.

Responsibilities

* Develops and executes annual marketing plan for product line(s) to ensure the achievement of financial/budget expectations and product line strategies.
* Effectively communicates business priorities to all functional areas to ensure goals are met.
* Responsible for product line marketing activities inclusive of pricing strategies, competitive analysis, promotional programs, market research requirements, strategic publication plans and channel strategies.
* Manages marketing communication programs including advertising, direct mail, product literature, sales tools, BD Internet sites, etc. in alignment with product line and brand strategy. Ensures timely communication to appropriate marketing and sales personnel relating to promotional materials and development of effective sales aids and clinical education support materials.
* Responsible for establishing and analyzing product pricing. Coordinates with Finance and Cost Accounting the provisions of accurate product costs in support of regional pricing and profitability planning.
* Provides product sales forecasts for use in production planning.
* Responsible for developing distribution and contract strategy for assigned products.
* Employs market research tools as required to identify and interpret changing user attitudes, demands, and needs for existing company and competitive products.
* Maintains optimal product portfolio through preparation and submission of new product proposals and selected product rationalization. Coordinates these activities with worldwide regions (as applicable), the service organization, Operations, and Supply Chain Management.
* Review product descriptions, technical specifications, product labeling and product packaging to ensure application information is appropriate for intended audiences and that information and design supports the product's brand strategy.
* Develops strategies and training plans pertaining to regional product launches for the service organization, distributors, and the direct sales force.
* Provides marketing and/or technical support at conventions, user's meetings, workshops and other specific marketing functions. Conducts demonstrations as required.
* Develops and executes plans to maximize business and communicate to sales force and customers during product constraints and technical product issues. Coordinate in conjunction with Quality, Operations, Technical Service, and Customer Services functions.
* May participate in BD's product development process.
* May support OEM relationships, as needed.
* Other responsibilities as assigned.

Qualifications

Required Knowledge, Skills and Abilities

* Requires a BS in related scientific discipline, marketing or business, MBA highly preferred. Four years of related sales or marketing experience.
* Minimum of 3 years of business experience in one of the following: marketing, product management, or business development. Experience in the medical device industry highly preferred.
* Has developed and implemented: pricing and branding strategies, advertising and public relations plans, and detailed marketing plans.
* Demonstrates ability to conduct, analyze and present financial evaluation of a project including IRR, EVA, MVA and NPV modeling and can present such models to others.
* Demonstrates effective communication and presentation skills.
* Has a history of achieving and delivering against key objectives and timelines.
* Able to work at a fast pace with minimal supervision or structure.

Job
Product Management

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Product-Manager-Job-MD-21201/655733/6557336557332010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
Description

Job Summary

Provides consultative business process and system support to BD Bioscience R&D, and other functional areas as needed. Analyzes business problems of a non-routine and complex nature. Provides technical expertise in identifying, evaluating and developing systems and processes that are cost effective and meet user requirements. Uses background and experience to work with users to identify root causes of problems related to enterprise business systems and applications that support or interface to them. Operates in a matrix organization, leading cross functional teams to address business and system issues.

Defines overall project strategy. Works with the business to identify and document business requirements, estimate tasks and timelines, and develop project plans. Manages all implementation processes including resource allocation, progress tracking, change control, testing, documentation and training processes from system initiation through delivery according to established time, scope, budget, resource and quality standards. Plans, performs and documents system integration and validation tests. Projects may vary in number, size, and complexity.

Duties and Responsibilities

* Acts as a consultant to the BD Bioscience R&D business in addressing process and system issues, through a combined understanding of business and technical concepts as they relate to business solutions.
* Designs and orchestrates the implementation of business processes and/or automated solutions to business problems.
* Troubleshoots technical issues where knowledge of design and technical structure is required.
* Applies problem analysis techniques and coaches the business to identify cost effective and high quality solutions.
* Collaborates and works across functional areas to ensure that solutions support cross-functional business processes.
* Plans, executes and tracks projects utilizing BD's project management methodology and tools.
* Communicates project goals, objectives, status and issues to the project team, business partners, and management.
* Understands working in a regulated environment; manages requirements for compliance in own area of work and complies with those requirements. Supports and maintains the validated status of systems using BD's System Development Life Cycle and validation methods and tools.
* Maintains technical expertise through self-initiated training and certifications in technical and business applications, project management tools and techniques and continuous improvement methods, such as Six Sigma.
* Promotes a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Notifies supervisor of all observed hazardous conditions on unsafe work practices.

Qualifications

Knowledge and Skills

* Solid overall understanding of ERP, CRM and/or Business Warehouse functionality, systems and processes as appropriate.
* Strong knowledge of system configuration, technical design and associated tools.
* Strong knowledge of the application of continuous improvement tools, such as Six Sigma, to business processes.
* Knowledge of project management tools and methodologies.
* Strong interpersonal and communication skills.
* Knowledge of R&D business process and related systems are considered an asset.
* Knowledge of the following platforms is considered an asset: ERP, LIMS, Content Management, Data Warehousing, Virtualization technologies, Collaboration technologies

Key Competencies

* Ability to reason and deal with ambiguity; can comfortably handle risk and uncertainty.
* Exhibits business acumen - Is broadly knowledgeable about business and technology and is able to relate this knowledge to our business strategy, market and environment.
* Makes good decisions, especially under deadlines or pressure situations, based on analysis, wisdom, experience and judgment.
* Builds effective teams, creating strong morale and team spirit; creates a feeling of belonging in the team.
* Priority setting - Knows and spends time on what is important; quickly zeros in on the critical few tasks and puts aside the trivial.
* Communication skills enabling clear and articulate speech and writing targeted to audiences that include senior management and/or outside organizations.
* Exhibits a bias-to-action and a focus on results rather than analysis-paralysis.
* Challenges prevailing assumptions when warranted and suggests better approaches; works to minimize complexity and simplify processes.
* Exhibits good judgment about which creative ideas and solutions will work and is objective and flexible to perspectives of others; listens well.

Education and Experience

* 5+ years experience in a business environment, with experience managing multiple projects
* A Bachelor's degree in a business or analytical discipline
* Experience in the functional development, deployment and maintenance of ERP systems is considered an asset
* Experience in Medical Device, Pharmaceutical or Biotech IT is considered an asset
* A PMI Project Management Professional (PMP) certification is considered an asset
* A Six Sigma certification is considered an asset
* Other appropriate industry certifications such as SAP or APICS are considered assets

Job
Project Management

Primary Location
US-California-San Jose

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-JOSE-Project-and-Process-Manager-Job-CA-95101/656891/6568916568912010-04-10BDfull-timeUSDstarting0BSSan Jose, CA, US
Description

Reporting to the Engineering Manager, Molding, Manufacturing Process Technology. Responsible for the project management of injection molding tool development in support of new medical disposable product activities. Carries out mold tool development from the prototype stage to full commercial scale tooling and does the process development required to support commercialization.

Responsibilities:


* Significant contributor to the development of technology strategy and plans for molding.
* Manages project activities, including planning, organizing, and execution of major projects to successful completion with emphasis on timing, budget, and business performance.
* Provides project management leadership for the injection molding tooling required to support a new product.
* Provides technology input to guide product development on design-for-manufacturability.
* Can be a team member or team leader on multi-functional project teams in support of new product launches.
* Interfaces with R&D, Marketing, Design, and Manufacturing in the execution of project goals.
* Responsible for the budget plan and execution in support of new product projects, including expense and capital equipment.
* Seeks and evaluates new technologies for application to BD Business.
* Provides leadership in the transfer of new mold tooling applications to manufacturing.
* Communicates and coordinates molding process development activities.
* Directs projects and/or employees in multi-functional setting. Directs activities of vendors and plant technicians to accomplish project objectives.
* Anticipates consequences of actions and/or decisions. Makes decisions that are in the best interest of the company. Seeks new methods/solutions to achieve goals; has the ability to react quickly to changing situations. Prepares and maintains specific project task load time commitments to meet appropriate priorities.
* Demonstrates initiative and innovation in action/ideas, respectively with constant vision toward execution of his/her assignment(s), including project management.
* Contributes to and participates in expense and capital budgeting. Prepares CB-2 for submission. Controls spending.
* Interfaces with appropriate/relevant functional groups and manufacturing sites for achieving project goals.
* Keeps abreast and maintains latest technological developments in areas of responsibility.
* Works independently to take work and get it done by prioritizing and scheduling the completion of assignments, within budget constraints.
* Has authority to prioritize required activities in order to achieve overall project (s) objective.
* Monthly status report to Manager and Director.
* Able to train, develop and counsel assistants and team members.

Qualifications

Education:

BS Mechanical or Plastics Engineering required; tool and die maker training preferred.

Experience:

Minimum of eight years experience in injection molding tool technology.

Knowledge of plastic part design.

Intimate knowledge of thermoplastic and thermoset technologies, molding materials

technology, and assembly technology.

Knowledge of plastic processing.

Knowledge of metrology techniques for plastic parts.

Knowledge of molding production operations in a high volume precision parts business.

Job
Project Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Senior-Project-Engineer-Molding-Job-NJ-07417/659509/6595096595092010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employee

About us

Description

Responsibility

Reporting to the Engineering Manager - Assembly, this position is responsible for new assembly and packaging equipment technology and procurement supporting new product introductions and capacity expansion from concept, to prototype and through commercialization of Sample Acquisition products/devices. This position will work closely with R&D, Marketing, Design and manufacturing plants to implement this manufacturing technology.

Job Description

Project Management

Responsible for the project management from concept through to commercialization of new process equipment, including but not limited to: -

· Resource and product cost planning

· Expense and capital spending plans and capital request development and submission

· Develops and executes the technical strategy to accomplish project goals.

· As required by the division business agenda, will be Core Team Member, leading and managing BD manufacturing strategy and project teams.

· Leads technical team of engineers and technicians and co-ordinates resources to achieve project and business goals.

Technical Skills

· Works with product design and development teams to ensure robust manufacturability of new products.

· Applies six-sigma and lean manufacturing methodologies from prototype design, machine design and build and through final validation to ensure optimization of new product lines.

· Requires an expertise in high speed metal and plastic parts feeding, assembly and parts joining.

· Must be able to successfully identify and apply new technologies and processes for a competitive advantage.

Financial Control

· Responsible for managing and tracking project resources within the defined project approval plan which includes but is not limited to: Capital procurement approved by the Fiscal Budget, Travel Expenses, Project Expenses, Training requirements for team members, and Allocated Labor Hours.

Equipment Procurement

· Request for assembly line quotes, vendor analysis and recommendation, and support for Contract Development

· Converts Design Input Requirements into machine specifications and acceptance protocols to purchase high-speed automation equipment.

· Manages vendors in the design, process development, timeline commitment and implementation of automation equipment.

· Supports Process Validation of Equipment in manufacturing Plant

Qualifications

Education:

* BS Mechanical Engineering

Experience:

* Minimum of ten years experience in high volume medical device, pharmaceutical, or food products industry.
* Experience in organizing and leading multi-functional team
* Demonstrated capability in project management, with experience on large capital projects
* Proven track record in high-speed automated equipment development in medical device or pharmaceutical industry preferred.
* Experience working in development environment with an understanding of process design process capability and manufacturing cost analysis.
* Estimate capital and product/process costs to support development programs.

Job
Program Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Senior-Project-Engineer-Assembly-Job-NJ-07417/659510/6595106595102010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Manages clinical trial operations of large and/or complex multicenter studies. Provides oversight and direction to members of a large, multidisciplinary project team throughout the conduct of assigned clinical trials, under the guidance of the Director of Clinical Operations/Affairs. Oversight accountability for Clinical Research Associates.

Principal Accountabilities:

1. Provides significant input into clinical and regulatory strategy sessions for assigned projects. Develops and implements clinical trial protocols and operational plans which are consistent with strategic corporate and departmental objectives and assumes primary accountability for the ongoing progress of those plans on assigned studies. Primary interface to clinical investigators and Key Opinion Leaders (KOLs), ensuring their input into protocols, reports, and publications.

2. Manages resources and timelines associated with all study start-up activities, including investigator agreements, central IRBs, regulatory documents, contractual agreements, and device shipment authorizations. Manages the identification, recruitment, and selection of investigators and testing laboratories for planned studies.

3. Ensures the appropriate development of study documents, including informed consent forms, case report forms and instructions, site selection materials, procedural manuals, project newsletters, and other project-specific documents required for the conduct of assigned studies with relatively little oversight.

4. Assumes primary accountability for assigned clinical trials and ensures compliance with applicable regulations, guidelines, and corporate policies for trial activities. In conjunction with the Director of Clinical Operations/Affairs and departmental working practices, ensures the development and maintenance of project-specific tracking systems to enable proper trial management and monitoring activities. Ensures operational and regulatory integrity of assigned trials by reviewing enrollment status reports, monitoring site visit reports, expense reports, memos to file, telephone contact reports, and CRO documentation.

5. Provides daily direction to CRO Project Managers and TriPath Clinical Operations/Affairs project team members as required to meet project objectives. Assumes primary accountability for ensuring that the Clinical Operations/Affairs team members meet the overall project objectives within the timelines and budgets established by the Director of Clinical Operations/Affairs and VP of Regulatory and Clinical Operations/Affairs. Develops and maintains detailed timelines and resource projections for assigned projects. Provides routine status reports and updates to the Director of Clinical Operations/Affairs regarding the progress of assigned studies.

6. In collaboration with the Director of Clinical Operations/Affairs, identifies and evaluates internal and/or external resources required for assigned clinical trials. Independently manages external partners for outsourced work.

7. Assumes primary accountability for planning and managing Investigator's Meetings, Project Training Meetings, Steering Committee Meetings, DSMB meetings, Adjudication Panels, etc. associated with assigned clinical trials. Represents TriPath Clinical Operations/Affairs Department as required.

8. Manages personnel responsible for the distribution of documents, forms, supplies, equipment, laboratory supplies, and study device required to execute clinical trials. Plans and implements study supply activities to ensure that all materials needed to execute the study are available when needed.

9. Serves as a manager to Clinical Research Associates assigning them to project(s) and maxtrixing with CTMs to ensure compliance with applicable Monitoring Plans, regulations, guidelines, and corporate policies. Has direct accountability for contract CRA with review and approval of monitoring reports and timesheets. Assigns contract CRAs to BD CRAs for BD monitoring oversight.

10. Assumes primary accountability for ensuring that internal project team members are trained appropriately to ensure proper study conduct.

11. Writes and oversees the creation of internal and external memos, reports, documents, and correspondence required to properly manage and document activities on the studies. Ensures maintenance of project files according to applicable regulations, guidelines, and corporate policy.

12. Interacts with Data Management personnel as needed to resolve data queries and lock the clinical database(s) quickly and efficiently. Interacts with Biostatistics and Medical Writing personnel as needed to analyze and report the study(ies). Authors final clinical report, in conjunction with Director of Clinical Operations / Affairs, including input from investigators and KOLs.

13. In conjunction with the Director of Clinical Operations/Affairs, plans, implements, and documents auditing activities on assigned projects. Participates in FDA inspections as required.

14. Serve as a resource/mentor to Clinical Trial Managers.

Job Dimensions:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

Language Ability:

Ability to read, interpret, and develop clinical protocols and all associated study materials. Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, and governmental regulations. Ability to write Clinical reports and protocols, business correspondence, and procedure manuals. Excellent communication skills including the ability to effectively present information and respond to questions from project teams, external vendors, clients, customers, and the general public. Prior experience working with investigators and Key Opinion Leaders required.

Operations Ability:

Ability to operationalize complex clinical trial programs by establishing and maintaining systems and processes necessary to control and report trial status and activities. Ability to manage project teams to ensure that quality, regulatory-compliant clinical projects are conducted on time and within budget.

Computer Skills:

Microsoft Project, Microsoft Word, Microsoft Excel , Internet software, E-mail, Database software

Supervisory Responsibilities:


The Senior Clinical Trial Manager serves as the matrix manager of team members assigned to large project teams and is responsible for carrying out KNOWLEDGE, SKILLS, AND ABILITIES in accordance with the organization's policies and applicable laws, as directed by the Director of Clinical Operations/Affairs. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. Senior Clinical Trial Manager has direct reports of CRA and SCRA and will assign them to project teams on a clinical trial. Additionally the SCTM has accountability for contract CRA monitoring report approvals, expense report approvals, and timesheets.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the ESSENTIAL FUNCTIONS of this job.

While performing the duties of this job the employee is occasionally exposed to fumes or airborne particles and toxic or caustic chemicals and human or animal tissue.

The noise level in the environment is quiet to moderate.

Accommodations:

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Qualifications

Education and Experience Required:

* Bachelor's degree in Medical Technology, biochemistry, or related life science field.
* Three years previous experience managing prospective clinical in vitro diagnostic (IVD) trials required.
* Experience managing project team personnel required.
* Three year minimum requirement managing people.
* Experience leading project teams through the start-up, trial conduct, data management, and report writing of FDA regulated prospective IVD clinical trials required.
* Knowledge of ICH guidelines, FDA regulations, and guidelines for clinical diagnostic trials required.
* Ability to work on problems of diverse scope where minimal direction is given for situational analysis. Ability to exercise judgment within broadly defined practices and policies to determine appropriate action. Normally determines methods and procedures on new assignments and provides guidance to lower level personnel.
* Ability to manage stringent deadlines required. Proven ability to provide solutions to a variety of technical problems of moderate scope and difficult complexity required.

Education and Experience Preferred:

* Higher education strongly preferred.
* Previous experience managing and designing PMA IVD clinical trials strongly preferred.
* Experience with site selection and managing international diagnostic clinical trials desired.
* Knowledge of international trial (evaluations) preferred. PMA trial experience strongly preferred.

Supervisory Responsibility:

* Matrix management of 4-40 multidisciplinary project team members, depending upon project assignment and number of contracted monitors.
* Clinical Research Associates will report directly to this position.

Job
Clinical Affairs

Primary Location
US-North Carolina-Durham

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/DURHAM-Senior-Clinical-Trial-Manager-Job-NC-27701/668271/6682716682712010-04-10BDfull-timeUSDstarting0BSDurham, NC, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Clinical Data Management Group Leader is responsible for the tactical execution of Clinical Data Management activities for Clinical Trials supported by BD Diagnostics - TriPath. Oversees data management and technical personnel in day-to-day activities while maintaining project schedules and high quality deliverables. Closely monitors resource allocation and work schedules, and provides input to performance reviews. Ensures adherence to quality system procedures, standards, and metrics. Sound data management judgment must be exercised within broadly defined regulations and internal procedures to achieve high quality and accurate clinical data.

Principal Accountabilities:

1. Leads and advises the group in design and execution of Clinical Data Management activities for Clinical Trials supported by BD Diagnostics - TriPath.
2. Reviews and approves work products to ensure consistency with standards and procedures.
3. Forecasts and monitors resource allocations.
4. Works with various businesses Clinical Operations functions for the execution of Clinical Trial activities.
5. Supervises and coaches Clinical Data Management and Technical associates.
6. Recommends and implements process improvement initiatives.
7. Demonstrates expertise in the use of commercially available Clinical Data Management Systems including Electronic Data Capture.
8. Provides guidance and expertise to Clinical Trials that are highly complex or novel to the group.
9. Ensures regulatory compliance for data management aspects of Clinical Trials.
10. Responsible for achievement of clinical project goals, project metrics, and agreed upon schedule.
11. Recruit, interview, and contribute to hiring decision for permanent, temporary, and contract staff.
12. Contributes to the development of department budgets and resource forecasting.
13. Performs data management tasks for Clinical Trials.
14. Provide necessary training to clinical associates.
15. Write reports and make oral presentations as required.
16. Normally receives no instruction on routine work, general instructions on new assignments.

Qualifications

Education and Experience Required:

* Bachelor's Degree required (computer science, life science, or related field)
* Minimum of 3-5 years experience in Clinical Data Management in Device Company or Contract Research Organization preferred. Pharmaceutical experience considered.
* 3 - 5 years experience in the following:
* working in a regulated industry, GCP, ICH, and ISO.
* device or drug development process.
* developing and/or using Commercial Off the Shelf Clinical Data Management Systems

* 1-3 years supervisory, mentoring, or team leader experience.
* Must be computer literate with working knowledge of relational databases and office software packages such as Microsoft Office, Excel, PowerPoint, and Project.

Education and Experience Preferred:

* Graduate Degree in computer science, life science, or related field
* Knowledge of regulatory requirements, FDA, ICH, GCP etc. guidance
* Strong interpersonal skills, demonstrated capability of working on multiple projects at one time.
* Knowledge in relational databases and office software packages.
* Demonstrated ability to work within a matrix organization.
* Strong problem solving skills and attention to detail.
* Good time management skills
* Expertise in: Clinical Data Management Systems, Electronic Data Capture and knowledge of Clinical Trial Management System.
* Must be computer literate with working knowledge of relational databases and office software packages such as Microsoft Office, Excel, PowerPoint, and Project.

Supervisory Responsibility:

* Supervises a Clinical Data Management Specialist

Job
Clinical Affairs

Primary Location
US-North Carolina-Durham

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/DURHAM-Clinical-Data-Management-Group-Leader-Job-NC-27701/668272/6682726682722010-04-10BDfull-timeUSDstarting0BSDurham, NC, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Description

This is a position encompassing dual responsibilities of operating a group of injection molding machines and training on setting up and adjusting a group of similar machines. Prime responsibilities will be for the quality and quantity of molded parts as well as safety, housekeeping, and paperwork.

1- Responsible for monitoring all auxiliary equipment for proper operation as well as following Quality Controlled Manufacturing Documents.

2- Responsible for performing dimensional and visual quality checks.

3- Responsible for the labeling of bags, boxes, or totes at the injection molding machines.

4- Responsible for proper handling and documentation of rejected product.

5- Train on the set up of assigned molds, machines and auxiliary equipment and monitor assigned work cells observing overall process and quality of molded parts.

6- Learn how to interpret the root causes of quality issues.

7- Perform minor repairs to molds, machines, and all auxiliary equipment.

8- Complete all required paperwork such as line clearance, mold history, process run sheet, and safety check sheet.

9- Learn proper material identification, placement, mixing, and numbering procedures.

10- Learn how to hook up hoppers, set-up and troubleshoot other various auxiliary equipment necessary for proper material usage.

11- Learn how to clean and maintain grinders.

12- Participate on safety, emergency response, and 5S teams and monthly Safety Meetings and other teams and meetings as required or requested.

13- Comply with all departmental attendance and performance policies.

14- Comply with all local, state, federal, and BD safety regulations, policies, and procedures including RCRA Hazardous Waste regulations.

15- Comply with all local BD quality policies, procedures, and practices through consistent application of sound quality assurance principles.

16- Be willing to work any shift when training is completed, a setup job is available, and satisfactory performance has been demonstrated in all items in career block CB2T.

17- Other duties as assigned.

Qualifications

Minimum Education: High school diploma or equivalent. Must be able to read, write and communicate in English and basic math skills needed. Communication skills are essential.

Minimum Experience: Two to four years of manufacturing experience (at least one year of injection molding machine experience preferred) and must be able to certify in Career Block One within three (3) months.

Job
Production

Primary Location
US-Utah-Sandy

Shift
Rotating

Relocation Available
No]]>http://www.bd-careers.com/job/SANDY-Process-Technician-Mold-Set-Up-Trainee-Job-UT-84070/672535/6725356725352010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
Description

JOB SUMMARY

Provides technical support for the engineering and manufacturing departments in the area of control system maintenance and troubleshooting, including such areas as PLC's, servo's, motor controls, vision systems, molding equipment and other related systems. Supports the engineering department in the area of control system programming and upgrades.

ESSENTIAL FUNCTIONS

The essential functions of this position include but are not limited to:

1. Diagnoses and correction of electrical and electronic malfunctions which are beyond the capabilities of Setup personnel.

2. Diagnoses and correction of PLC and related control system malfunctions as well as installs, tests, repairs, and adjusts other electrical and electronic equipment such as recording, regulating, indicating and controlling instruments.

3. Repairs existing electrical parts and initiates purchase requisitions for components or supplies as appropriate.

4. Supports engineering initiatives for the development of new or upgraded control systems utilizing such technologies as Servos, PLC's, vision systems, motor controls, molding equipment, and other related systems.

5. Supports production personnel for machine repair and overhaul as needed.

6. Advises Parts Crib Attendant of parts needed for immediate use or for stocking locations.

7. Performs preventative maintenance as scheduled.

8. Proposes design changes to supervisor in the areas of equipment upgrade, problem elimination, quality improvements and reduced costs.

OTHER RESPONSIBILITIES

Other responsibilities of this position include but are not limited to:

1. Complies with all local, state, federal and BD safety regulations, policies/procedures.

2. Complies with all local BD quality policies/procedures/practices through consistent application of sound Quality Assurance principles.

3. Performs other job related duties as assigned.

4. Observes all safety, environmental, and quality system standards.

All requirements are subject to possible modification to reasonably accommodate individuals with disabilities.

Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other employees.

This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by their supervisor.

Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the incumbent will possess the abilities or aptitudes to perform each duty proficiently.

This document does not create an employment contract, implied or otherwise, other than an "at will" employment relationship.

Qualifications

EDUCATION, EXPERIENCE AND SKILLS REQUIRED

1. Education

Requires a two-year degree from a technical school in electrical or electronic field.

2. Experience

No experience required, however, more than 1 year of experience in troubleshooting PLC and related control systems is preferred.

3. Physical Requirements

Medium-Heavy work: Exerting up to 75 pounds of force occasionally and/or up to 35 pounds of force frequently, and/or up to 20 pounds of force constantly to move objects.

4. Mental Requirements

Ability to read, write and understand English.

5. Equipment Use

Ability to operate computer, fork truck, pallet truck, small hand tools, electronic test equipment, etc. in successful completion of tasks. Must be a licensed forklift operator.

6. WORKING CONDITIONS

The worker is subject to both environmental conditions: Activities occur inside and outside.

Worker is subject to noise: There is sufficient noise to cause the worker to shout in order to be heard above the ambient noise level.

Worker is subject to vibration: Exposure to oscillating movements of the extremities or whole body.

Worker is subject to hazards: Includes a variety of physical conditions, such as proximity to moving mechanical parts, electrical current, working on scaffolding and high places, exposure to high heat or exposure to chemicals and broken glass.

Worker is subject to atmospheric conditions: One or more of the following conditions that affect the respiratory system or the skin: Fumes, odors, dusts, mists, gases or poor ventilation.

Worker is subject to oils: There is air and/or skin exposure to oils and other cutting fluids.

7. Supervision

Reports directly to the Process Engineering Supervisor. Has no supervision over others.

8. On the Job Training

On the job training for new hire technicians will consist of time spent with fellow technicians and

engineering personnel working on the floor with various processes. Time will be spent explaining the product flow through the plant and the function of each different process. An overview of the various technology platforms will be discussed as it relates to each of the different processes. Training will be performed on specific procedures for technicians such as Software Change Control. On the job

training my be performed both during dayshift hours and off shift hours on the individuals
respective work schedule.

Job
Technician

Primary Location
US-Nebraska-Broken Bow

Shift
Third Shift / Overnight

Relocation Available
No]]>http://www.bd-careers.com/job/BROKEN-BOW-ELECTRICAL-MECHANICAL-TECHNICIAN-Job-NE-68822/672536/6725366725362010-04-10BDfull-timeUSDstarting0BSBroken Bow, NE, US
Description

Position Summary:

The Clinical Project Lead (CPL) is responsible for leading the planning, negotiating, scheduling initiating and monitoring of clinical trials of moderate to high complexity in the women's health and /or sexually transmitted diseases field. The CPL leads internal and external CRAs to ensure compliance with device and PMA regulations and smooth conduct of clinical trials. The CPL is responsible for preparing reports of study results for investigators, assisting in preparation of regulatory submissions, and supporting publication activities. The CPL will interface with appropriate internal individuals to manage trials in order to meet business objectives and timelines, provide clinical and technical support to product development activities, support product launches, and/or conduct post-market surveillance and evaluation activities.

The position reports to the Medical Manager, Medical Affairs. The CPL is responsible for leading the execution of complex clinical projects and must work both independently and in a team environment.

Functional Responsibilities:


1. Responsible for leading planning, budgeting, executing, and monitoring clinical evaluations of BD products to support product development. Clinical evaluations may also be for post-market surveillance studies, or claims extensions of existing products.

2. Uses past clinical experience to support project planning and execution related to medical procedures performed during clinical trials related to women's health projects.

3. Activities will be performed in accordance with international, federal and/or local regulations (FDA, ISO), Good Clinical Practices (GCPs), and compliance with corporate and local quality policies and procedures.

Specific Responsibilities:

* Manages all activities related to multi-center trials.
* Coordinates activities with contract research organizations (CRO).
* Leads project-related activity of internal and external Clinical Research Associates.
* Screen, select, and qualify principal investigators and investigational sites.
* Conduct negotiations of clinical site budgets and contracts.
* Conducts "monitor training meetings".
* Coordinates monitoring visits and reviews monitoring reports.
* Mentor more junior clinical operations personnel.
* Ensure the compliance to all human subject protection and privacy regulations, including developing Informed Consent materials.
* Conducts feasibility (interviews investigator and/or CRC, assesses investigator's ability to meet enrollment requirements, etc..).
* Monitor clinical data and identify trends. Participate in data analysis planning.
* Develop medical project schedule and track tasks and provide back-up strategies to meet overall project schedule.
* Plan availability of supplies and shipment of materials.
* Coordinate training of clinical evaluation participants in study products and procedures.
* Monitor sites to assure that the Protocol is understood and followed.
* Communicate results of data analysis to each clinical center and actively support the publication and presentation of results by investigators.
* Support the reporting of performance data to regulatory authorities.
* Anticipate 25%-35% travel (primarily domestic; international travel a possibility).

Qualifications

Education and Experience

* BSN with clinical nursing
* Minimum 5 year in project management experience
* Five or more years experience in clinical trials in the medical device industry or in oncology device trials preferably in a CRO environment or with a device sponsor with PMA experience.
* Clinical Research Certification is preferred

Knowledge and Skills

* Deep knowledge of device regulations including PMA regulations. Working knowledge of Good Clinical Practices, human subject protection regulations, safety data monitoring,
* Must have excellent interpersonal, presentation, writing and communication skills.
* Must have strong knowledge of scientific study design and data analysis.
* Must have strong computer skills (MS Office, including Project, Word, Excel, Access, PowerPoint, ) -- prefer working knowledge of statistics and data analysis- preferred skills in database management.
* Ability and willingness to travel to domestic (and possibly) international locations as necessary (anticipate 25%-35% travel)

Job
Clinical Research & Trials

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Clinical-Project-Lead-Job-MD-21201/673432/6734326734322010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
Description

Responsibilities include (partial listing):

* Operators have complete responsibility for their quality, production, waste, and machine workability/accountability.
* Understand and operate inspection & testing equipment. Operators are responsible for identifying and correcting any dimensional defects and cosmetic defects according to current QC specifications, to insure good quality.
* Participate in training of new operators
* Perform scheduled and unscheduled machine maintenance and housekeeping.

Qualifications

Operators monitor, operate, and maintain two (2) glass syringe forming machines in line with other equipment (printer or Luer module), inspection equipment, and ovens. Desired skills, knowledge, experience:

* Teamwork, communication skills, mechanical aptitude troubleshooting.
* Training - operators must complete the training program and certification process.

Job
Production

Primary Location
US-Nebraska-Columbus East

Shift
Rotating

Relocation Available
No]]>http://www.bd-careers.com/job/COLUMBUS-Luer-Forming-Set-Up-Operator-B-Shift-Job-NE-68601/674255/6742556742552010-04-10BDfull-timeUSDstarting0BSColumbus East, NE, US
Description

Has overall responsibility for four injection manufacturing plants in the United States and the Drogheda Ireland flush operation. Provides overall leadership for the world wide cannula manufacturing operations. Lead the operating strategy for the Flush Business. Drives leaders in areas of responsibility to leverage key talents and skills among locations. Has direct responsibility for 4 Plant Managers. Manages the planning and deployment of capital investments and process development activities across all areas of responsibility. Works to facilitate a smooth and rapid transfer of new products and technology flowing out of R&D into the appropriate manufacturing location. Responsible for learning and development of manufacturing associates across the company. Building bench strength, sharing best practices, creating learning opportunities, and ensuring career development are priority activities.

Injection and Flush site locations - Las Piedras Puerto Rico, Franklin Wisconson, Columbus Nebraska, Canaan Connecticut, and Drogheda Ireland

Responsibilities will include:

1. Meeting Operational Objectives - Volume, Financials, Environmental Health and Safety, and Quality

2. Building long term capabilities aligned to business and platform needs. Will need to facilititate the close coordination of multiple Platforms and Manufacturing Plants.

3. Driving Value Stream Improvements and improving upon variability.

4. Provide leadership in developing people capabilities across areas of responsibilities

5. Lead, develop and manage an effective Capital Plan for areas of responsibility

World wide Cannula manufacturing plants - Juiz de Fora Brazil, Columbus Nebraska, San Luis Potosi, and Tuas Singapore

1. Drive the capability build of people and process

2. Driving Value Stream visibility & improvements while removing variability within and between the Cannula manufacturing Plants.

3. Establish and maintain a robust Cannula contingency planning

4. Oversee and manage the Capital Plan for all Cannula Plants.

WW Flush Operations Strategy

1. Developing and helping drive the Flush Operations Strategy.

2. Develop and Manage the Capital Plan for world wide Flush Capacity Increase. Execute the world wide Operations Strategy for Flush and prepare other world wide locations.

Qualifications

Minimum Education:

* BS Degree in Business, Engineering or Industrial Management
* MBA or graduate engineering degree is strongly desired

Minimum Experience:

* 15 years of progressive leadership, budgetary, and scope of responsibility required
* Must be visionary and have broad business knowledge in manufacturing, engineering, supply chain, human resources and finance.
* Must possess good interpersonal, coaching and communication skill to work effectively across geographies and cultures.
* Able to coordinate numerous programs and activities across multiple manufacturing sites.
* Experienced in strategy development, product development, process development, sustaining engineering and new product launch activities.
* Must be expert in the application and use of Continuous Improvement tools and methodologies
* Working Knowledge of ERP Systems (SAP), FDA, GMP and ISO Regulations
* This position requires a minimum of 10 Years experience in medical devices, including 5 to 10 years experience leading large manufacturing organizations.

Job
Manufacturing

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-VP-Manufacturing-Injection-Job-NJ-07417/677516/6775166775162010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
Description

This position is part of the Operations Organization for the BD Diagnostic Systems Segment and reports directly to the Packaging Engineering Manager. This position supports the primary organization strategic areas by driving growth through the development and implementation of innovative packaging solutions and by funding growth through initiating and supporting cost savings and standardization efforts. The role is cross-functional in nature working closely with Manufacturing, Procurement, Marketing, Quality Management, Regulatory Affairs, R&D and Distribution as well as external packaging suppliers. This function combines technical expertise, project management and cross functional team skills to provide a complete source of packaging services.

* Responsible for packaging related projects and packaging types in assigned categories to include: package design, packaging process development and optimization, cost reductions and supporting manufacturing efficiency efforts as well as identifying packaging related defects and driving resolution.
* Lead the conceptualization, initiation, development, and commercialization of new and improved packages and processes including design generation, prototype development, specification development, functionality testing, and mold qualifications as necessary. This would include the coordination and implementation of primary, secondary and tertiary packaging from concept to implementation.
* Manage and lead packaging projects effectively and professionally to ensure agreed upon key business objectives and product launches are met. This would include leading multi-functional teams as appropriate.
* Provide timely package engineering support for development and ongoing production needs of all packaging materials related to the manufacturing of related products.
* Ensure package and product compatibility by identifying and executing package performance testing.
* Specification development and component validation are core competency requirements.
* Develop, justify and execute capital projects related to packaging (i.e. molds)

Qualifications

Required Knowledge and Skills:

* Solid communication skills, both written and verbal, which deliver information as well as clear positions on issues to be addressed and potential solutions.
* Strong leadership and project management skills which include project plan development and management as well as maintaining project budgets.
* Ability to determine priorities based on key business objectives and management of multiple projects simultaneously.
* High degree of creativity and ability to work independently yet collaboratively with other functional areas.
* Ability to interact well with peers, subordinates and senior personnel in multi-disciplinary teams.

Required Education and Experience:

* BS in Package Engineering, or related discipline, required.
* Minimum 5 years experience with packaging materials and package development, preferably in a FDA-regulated industry.
* Minimum 5 years experience with some combination of packaging systems / materials preferred including: Extrusion and Injection Blow molding, Injection molding and/or glass molding, bottle / cap configurations, laminated structures, folding cartons, corrugated and labeling.
* Minimum 5 years experience with some combination of, liquid filling equipment, heat sealing, molding, thermoforming and / or sterilization processes preferred.
* Proficient in: Microsoft Office (Excel, Word, Power Point) Highly preferred: Palletization Software (ie.CAPE) , AutoCAD / Solid Works as well as and Microsoft Project. HAZMAT (hazardous materials) experience and training is desired.

Job
Packaging Engineer

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Sr.-Packaging-Engineer-Job-MD-21201/680063/6800636800632010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Responsible for the preparation of regulatory submissions required to market new or modified medical devices and in vitro diagnostic devices in both domestic and international clinical markets. This responsibility entails development, execution and management of procedures and systems designed to ensure that the product development process, including clinical studies, addresses all regulatory requirements as well as the objectives of the business.

Understands and interprets U.S. and international medical device and in vitro diagnostic device (IVD) regulatory requirements; provides guidance on requirements to product development teams. Develops strategies for submissions to FDA and other regulatory agencies. Provides risk assessments and regulatory options. Prepares U.S. regulatory submissions necessary for new product market clearance/approval and product continuance: 510(k)s; Pre-market Approval Applications (PMA) and supplements; Investigational Device Exemptions (IDE). Prepares and/or compiles information required by ex-U.S. regulatory associates to register or license products outside the U.S.

Interacts and negotiates with U.S. regulatory agencies. Coordinates the preparation of additional data/information requested by regulatory agencies and prepares appropriate responses to all such requests. Participates in the development and review of product release documents.
Reviews clinical protocols to assure collection of appropriate data for regulatory submissions. Periodically monitors status of clinical studies and reviews analysis of resultant clinical study data. Based on these data and considering the regulatory requirements, recommends appropriate courses of action. Reviews labels, labeling, and promotional materials for compliance with applicable regulations and policies.
Provides regulatory opinions on premarket regulatory requirements, export, and labeling requirements

Qualifications

* Current knowledge of U.S. medical device and in vitro diagnostic regulatory requirements, Good Laboratory Practices (GLP) and Quality System Regulations (QSR); current knowledge of European Medical Device and IVD Directive requirements and European quality system standards.
* Ability to effectively communicate both verbally and in writing to all levels within the organization and external to the organization.
* Ability to organize work; project management experience desirable.
* B.S. degree in the biological sciences, chemistry or related science required.
* 3 years experience in the device/diagnostic, biologic and/or pharmaceutical industry, primarily in the area of regulatory affairs.

Job
Regulatory Affairs

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/BALTIMORE-Regulatory-Affairs-Specialist-Job-MD-21201/680072/6800726800722010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD Biosciences, a segment of BD, is one of the world's leading businesses focused on bringing innovative research and clinical tools to life scientists and clinicians. Its product lines include: flow cytometers; cell imaging systems; monoclonal antibodies; research reagents; diagnostics assays; and tools to help grow tissue and cells.

About us

Description

Working out of Billerica, MA and reporting to the Technical Support Manager, the Applications Specialist will support the DL Marketing plan by focusing on key applications work (laboratory work, development of application notes, external collaborations with opinion leaders) and outbound Marketing support. The Applications Specialist will provide advanced applications support to address key business objectives pertinent to Marketing and Technical Support, to include developing and writing technical content for publication in marketing literature and external publications (including results of laboratory work), performing competitive benchmarking, identifying major technical trends and communicating respective information to key functions, and developing and presenting focused technical seminars at various customer forums.

KNOWLEDGE AND SKILLS

· Advanced level knowledge of cell biology (including stem cell biology)

· Excellent communication skills, both written and oral; excellent interpersonal skills

· Computer literacy required; i.e. PC software, databases, documentation software

Qualifications

EDUCATION AND EXPERIENCE

· Bachelors degree in Cell Biology or related field, Masters preferred

· 5-10 years research experience is required

· Experience in business/customer aspects of the cell biology field is preferred

· Experience in the area of high throughput screening is a plus

Job
Other

Primary Location
US-Massachusetts-Billerica

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BILLERICA-Applications-Specialist-Job-MA-01821/680743/6807436807432010-04-10BDfull-timeUSDstarting0BSBillerica, MA, US
BD Biosciences, a segment of BD, is one of the world's leading businesses focused on bringing innovative research and clinical tools to life scientists and clinicians. Principal product lines include fluorescence activated cell sorters and analyzers; cell imaging systems; monoclonal antibodies and kits; research reagent systems; tools to aid in drug discovery and growing tissue and cells; and diagnostic assays. Its customers are involved in basic research, the discovery and development of drugs and vaccines, clinical trials, diagnostic testing and disease management. This diverse customer base includes academic and government institutions, pharmaceutical and biotech companies, and clinical laboratories.

BD BIOSCIENCES IS AN EQUAL OPPORTUNITY & AFFIRMATIVE ACTION EMPLOYER

About us

Description

The role of the Clinical Research Associate involves planning, supporting, implementing, and reporting the results of BD Immunocytometry Systems Medical Affairs clinical trials and other programs. This includes activities such as preparation of clinical plans protocols for evaluations of new products and the execution of these activities. These evaluations will characterize performance of a product relative to specific applications and intended uses to support regulatory submissions to government agencies (US and global). Additional activities will include post-marketing studies and/or clinical research evaluations. The Clinical Research Associate works independently on problems of moderate complexity, follows standard procedures and practices, and exercises judgment within a defined scope. He/she receives general instructions on routine work, and detailed instructions on new assignments.

Qualifications

Qualifications:


* A minimum of a Bachelor's degree
* A minimum of 3 years clinical trial experience in the in vitro diagnostic, medical device, pharmaceutical, and/or biotechnology industry.
* A minimum of 2 years hands-on laboratory experience

Assets:


* Individuals with a degree in Immunology, Biology, Microbiology, or Medical Technology are preferred.
* Advanced degree preferred.
* Pharma experience a plus
* Project leadership experience a plus
* Effective interpersonal skills.
* Effective work planning and organizational skills including budgeting for material requirements.
* Demonstrated ability to perform detail oriented work with a high degree of accuracy.
* Effective written and oral communication skills.
* Effective negotiation skills.

Job
Clinical Research & Trials

Primary Location
US-California-San Jose

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-JOSE-Clinical-Reasearch-Associate-Job-CA-95101/681975/6819756819752010-04-10BDfull-timeUSDstarting0BSSan Jose, CA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Works on assignments that are moderately complex in nature where ability to recognize deviation from accepted practice is required. Uses judgment requiring location and storage of items, proper packaging, methods of movement of materials, and release of materials. Ability to work independently as required. May receive general supervision with little instruction on routine work. May coordinate and/or execute special projects as required by the Department. Performs administrative and physical tasks involved in shipping, receiving, storing and supplying materials (raw, work-in-process, and finished goods), parts, and supplies, to operators, work stations and distribution center. Uses hand/or electric trucks including forklifts, Turret Trucks, Order Picker and other motorized vehicles requiring licenses. May prepare goods for final shipment (domestic and international). Keeps accurate logs (both written and on computer). Is knowledgeable of receiving and/or distribution function, packaging equipment and UPS systems. May require familiarity with sampling and inspection procedures and assisting in the monitoring of the quality of finished product in accordance with cGMPs (current Good Manufacturing Practices). May be responsible for conducting cycle counts to maintain accurate inventories. May train and implement functions in SAP. Effectively works in a team setting, supporting team goals and objectives. Make effective decisions relative to position requirements.

Qualifications

* Reading, writing, and basic arithmetic skills required.
* Ability to safely operate all required equipment and use packaging equipment, UPS and/or computer systems is required.
* Must be able to pay continuous attention to detailed operations requiring some diversification in approach to fairly routine processes.
* Lifting or moving of 5-25 lbs. continuously, 25-60 lbs. frequently, is required.
* High school diploma or equivalent and 1-2 years experience required.
* Forklift license required OR ability to obtain license within one month of hire.
* Basic proficiency with PCs (Personal Computers) and basic use of a Windows environment is required.

Job
Manufacturing

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Material-Handler-III-Job-MD-21201/681976/6819766819762010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

With limited direction from the Platform Leader and the Senior Director of World Wide Operations Diabetes Care, the Manufacturing Integrator is responsible for developing and supporting the Operational Strategy for the platform team by:

· Assisting and supporting the platform team in achieving their strategic and financial objectives.

· Supporting new product development activities by providing leadership, analysis, technical support and recommends effective solutions to operational issues to improve cost, revenue and asset utilization.

· Developing, maintaining and coordinating the tracking of major operational metrics, ie balanced score card and makes improvements as needed to remain aligned to business needs and priorities.

· Providing the support necessary to maintain key business operational imperatives. In carrying out these responsibilities, the Manufacturing Integrator coordinates activities by interfacing with the leadership in BD manufacturing facilities, the leader of assigned Business Unit(s), Senior Management in the Manufacturing Operations organization, various functional leaders within BD (Finance, R&D, for example) and external suppliers / vendors.

Operations lead for the Platform Leadership Team, responsible for development and implementation of the overall Platform strategy with the other members of this team.

Assist in the development of manufacturing plans to meet the objectives and strategies of the Diabetes Care business strategy; and formulates manufacturing plans to meet these objectives. Provides cost and capital estimates, make vs buy analysis, evaluations of alternatives and makes recommendations to achieve results.

Works with Platform Teams and the Supply Chain organization in assessing capacity needs, developing capacity and sourcing plans, and in developing worldwide manufacturing strategies. Proactively communicates across these organizations while taking a leadership role in executing the strategy.

Collaborates with Plant managers, Process Development, R&D, and others to develop manufacturing project and startup ramp up plans for new products.

Makes recommendations and manages the transfer of Diabetes Care manufacturing processes, equipment and technology across the global BDX and external supply partner manufacturing network.

Develop and initiate CB-2 capital requirements for manufacture of new products. Works with plants, R&D, finance and Platform leaders in the development and approval of CB-2's recommending capital expenditures and their financial justification. Provides analysis and narrative outlining project objectives, scope, and timing. Provides capital planning information and monitors capital spending to ensure compliance to targets and forecast.

Provides analysis and technical support in the assessment and assignment of a product or product line to manufacturing plants. Makes location recommendations based on manufacturing cost, technology fit, facilities requirements and availability, and equipment /process requirements.

Maintains awareness of state-of-the-art technology applicable to assigned programs by participation in professional societies, attendance at technological meetings and seminars and development of professional contacts.

Incumbent executes responsibilities with a large degree of autonomy requiring minimal day-to-day oversight by immediate supervisor.

Incumbent must engage and gain the support of associates in various positions of responsibility and in various functions within BD worldwide. This includes associates in these functions who occupy positions of authority that is equal to, greater than or less than the incumbent. Incumbent must clearly communicate project plans and resource requirements to gain the support of these individuals.

Incumbent deals with a wide variety of processes including assembly and inspection methods, packaging and sterilization of which any combination must meet the integrated requirements of medical use, chemical / biological compatibility, manufacturability, and acceptable cost.

Incumbent represents BD when interfacing with external vendors / suppliers as processes are developed and capital equipment is purchased.

All activities are conducted in compliance with applicable standards and regulations

Qualifications

· Requires minimum B.S. Mechanical or other relevant engineering discipline plus 8-10 years experience in project management and the design / implementation of manufacturing equipment / processes. Experience in the area of Medical sterile disposable devices is preferable. Experience in working with equipment suppliers and all levels of manufacturing plant personnel.

· Incumbent must understand the overall business strategy of assigned business and be able to structure and implement an Operations strategy to support this Business strategy with potential annual sales in the range of $40 - $400 million.

· Strategic grasp of manufacturing best practices, state of the art manufacturing technology and deployment of such.

· Ability to work and influence decision-makers across multiple sites/regions/levels of manufacturing sophistication.

· Knowledge of the interrelationship of Manufacturing Operations and Finance, Quality, Regulatory and Supply Chain in an FDA/ISO regulated environment. Experience in interfacing with these functions to achieve objectives.

· Experience in preparing equipment specifications, capital appropriations and process validation documentation.

Job
Manufacturing

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Manufacturing-Integrator,-Diabetes-Care-Job-NJ-07417/684280/6842806842802010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD Biosciences, a segment of BD, is one of the world's leading businesses focused on bringing innovative research and clinical tools to life scientists and clinicians. Its product lines include: flow cytometers; cell imaging systems; monoclonal antibodies; research reagents; diagnostics assays; and tools to help grow tissue and cells.

BD Biosciences is an Equal Opportunity/Affirmative Action Employer

About us

Description

Associate Medical Director, Leukemia and Lymphoma (L&L)

BDB Biosciences

The Associate Medical Director, L&L, reports to the VP Medical Affairs and Clinical Operations and is responsible for overseeing all Clinical Operations and Medical Affairs activities associated to ongoing and future L&L clinical programs. The Clinical Operations activities will include supporting the L&L clinical projects, clinical study designs and clinical trials in conjunction with the Director of Clinical Operations. Additionally, the Associate Medical Director is responsible for strategic interactions with R&D, Marketing, Regulatory Affairs and Core teams and provides medical input, perspective and vision to the senior leadership team. The Medical Affairs activities will include interactions with key experts and opinion leaders in hematopathology (e.g., Investigator Initiated Studies), professional societies, as well as defining and executing a strategy for scientific publications and product investigations.

Primary Responsibilities:


* In collaboration with the VP Medical Affairs and Clinical Operations, oversee the management of all aspects of Medical Affairs and Clinical Operations in the L&L field.
* In collaboration with the Director of Clinical Operations, ensure delivery of optimal outcomes in L&L clinical trials, meeting objectives on-time, within budget and of the highest quality.
* Provide ongoing strategic insight to the leadership team regarding research and industry trends and business opportunities.
* Provide training and support to the organization related to clinical and relevant commercial aspects in L&L and ensure high quality scientific and core message integrity.
* Lead and coordinate Investigator Initiated Studies in support of product positioning, market development, relevant basic and clinical research, including review of protocols and draft publication manuscripts.
* Actively participate in functional and cross-functional meetings and contribute to the development of current and anticipated business opportunities.
* Serve as the company's hematopathology expert at external scientific and industry meetings.

Qualifications

Qualifications:


*
PhD degree

*
5 years of hematology/hematopathology in a lab environment

*
3 years of experience utilizing and interpreting flow cytometry data

*
2 years of experience overseeing or conducting clinical trials

*
Minimum of 1 year experience managing others

The ideal candidate will have:

*
Doctor of Medicine (MD) highly desired

*
US Board Certified Hematopathologist

* Minimum of 2 experience with conducting and/or overseeing relevant research studies
*
Minimum of 2 years of direct experience conducting clinical trials

* Minimum of 2 years experience with medical education activities, congress and symposia, and curriculum development meetings.
* Significant writing and content development experience.
* Up to 25% travel.

Job
Clinical Research & Trials

Primary Location
US-California-San Jose

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-JOSE-Associate-Medical-Director-Job-CA-95101/685222/6852226852222010-04-10BDfull-timeUSDstarting0BSSan Jose, CA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The Primary Care Sales Consultant is responsible for selling the Medical Surgical Systems' product portfolio to the US alternate site healthcare market segment. The portfolio includes Injection, Infusion, Surgical Blade, Scalpel, and Anesthesia product lines. The customer base is comprised of various alternate sites and US hospitals that are below 100 beds in size. The alternate sites include independent ambulatory surgery centers, large specialty clinics, pain management centers, public health departments, primary care physicians, long-term care, and academia.

The Alternate Site Sales Consultant manages his/her territory according to a FOCUS Account strategy, calling on the top 50 accounts according to existing business and revenue potential. An extended customer reach is achieved through collaboration with Distributor Sales Representatives, the Telesales function, and other forums

Primary responsibilities include: (1) Meeting/exceeding sales budget for assigned territory; (2) managing incremental conversion opportunities from initial targeting, through evaluation, product ordering, and inservicing; (3) maintaining existing business; (4) implementing Marketing initiatives; (5) implementing national/regional contractual agreements; (6) providing routine performance reporting; (7) working collaboratively with members of MSS Regional team and across BD units with other BD field associates; (8) working with local distributor branches servicing the territory; (9) utilizing available sales support resources; and (10) exemplifying the BD core values

Qualifications

* Must have a minimum of three years experience as a sales professional. Bachelors degree in business or life sciences required; MBA a plus.
* Excellent communication, interpersonal and analytical skills a must.
* Must have a demonstrated successful sales track record, solid negotiation skills, understanding of buyer/decision maker types, exhibit effective selling, listening, and verbal/presentation skills, and ability to assess and respond to customer needs.
* Must be proficient in Microsoft Word, Excel and PowerPoint.
* Former clinical experience preferred.
* Must have demonstrated experience in managing both internal and external budgets and resources, conducting pre-call planning, and ability to prioritize and segment accounts.
* Must be willing to travel at least 25%

Job
Field Sales

Primary Location
US-Pennsylvania

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/Field-Sales-Consultant-Primary-Care-(Pennsylvania)-Job-PA/687226/6872266872262010-04-10BDfull-timeUSDstarting0BSUS-Pennsylvania
Description

Job Summary:

The Product Manager - Software is responsible for product management activities required to implement and administer Business and Unit objectives for assigned product line(s), to include a focus on software / data management systems. Develops and maintains product marketing plans to exceed unit revenue and profitability goals for assigned product line(s).

Establishes and maintains a leading competitive position through strategic identification and tactical implementation of marketing opportunities.

Develops promotional and communication programs. Maintains a worldwide communications network with regional product / marketing managers to establish global best practices in software product management and marketing activities. Facilitates regional introduction of product launches.

Primary assignment to the offices in Sparks MD, with field-based activities approximately 30% of the time.

Duties and Responsibilities:


Product Management

· Develop and execute annual marketing plan for assigned product line(s) - software / data management systems - to ensure the achievement of financial / budget expectations and product line strategies.

· Execute product line marketing activities inclusive of promotional programs, and market research requirements

· Manage centralized marketing communication programs including advertising, direct mail, product literature / sales tools, and BD internet sites in alignment with product line and BDDS brand strategy.

· Ensure timely communication to appropriate Marketing and Sales personnel relating to promotional materials and development of effective sales aids and clinical education support materials.

· Execute training plans pertaining to regional product launches for Sales, Service, and Distribution.

· Acts as worldwide liaison with regional product managers for pricing guidance, new product proposal preparation, and catalog and inventory management.

· Manage the coordination with regional marketing and product management colleagues to ensure operations activities (e.g. inventory, catalog) are established and operational, in order to execute to the tactical plan goals.

· Responsible for managing OEM relationships, as needed.

· Provides marketing and / or technical support at conventions, users' meetings, workshops, and other specific marketing functions.

New Product Development

· As a Marketing representative, assist as needed with product concept preparation for software / data management systems enhancement and new module development. Contribute requirements and technical expertise.

· Responsible for outbound marketing activities on product line(s) development core team.

Qualifications

Required Knowledge, Skills, and Abilities

· Minimum of 3 years business experience in marketing, product management, and / or business development. Business experience may include marketing, sales, related scientific discipline, IT or software engineering.

· Experience in the medical device industry and / or healthcare informatics industry highly preferred.

· Demonstrated understanding of product lifecycle management and new product development initiatives from idea generation and developing product requirements, through market launch.

· Must possess excellent written and verbal communication skills.

· Ability to work in a globally focused environment, internationally and across various regions.

· Effective presentations skills (including use of appropriate technologies) encompassing peer group(s), sales organizations, senior management, and customers.

· Ability to travel up to approximately 30% of the time, as needed

Required Education:

· BS in Marketing, Business, or related scientific discipline.

· MBA highly preferred.

Job
Product Management

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Product-Manager-Software-Job-MD-21201/689717/6897176897172010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
Description

Accountable for all marketing activities supporting a Product Line within a Business Platform of the Medical Surgical Systems Business Unit. Responsible for full life cycle management of the Product Line. Actively participates in the development of the Product Line and platform global strategies. Establishes key customer relationships. develops customer requirements, and proposes new product concepts. Conducts Market Research. Acts as Voice of Customer in all decisions related to the Product Line. Supports product development activity for the extension and expansion of the Product Line and establishes claims. Launches and promotes products through conferences, literature, clinical trials, and collateral development. Responsible for managing and providing support on existing marketed products and interfacing globally with internal and external customers. Acts as owner of Product Line, ensuring maintenance of quality, regulatory, and manufacturing compliance. Establishes sales budgets. Creates marketing campaigns to drive financial performance. Benchmarks competition and stays fluent with state of the art in clinical practice. Conducts detailed analyses of the Market and Sales Performance. Crafts impactful Business Models and Marketing Plans. Presents work to Senior Leadership.

RESPONSIBILITIES

1. Strategy and Business Development

· Support development of Business Unit and Business Platform Strategy

· Identify trends in clinical practice, technology, regulatory pathways, and customer behavior.

· Source and sense new concepts and ideas.

· Benchmark competition

· Identify and conduct initial diligence on new business relationships

2. Product Development

* Define product concepts and author customer requirements.
* Lead cross-functional product development teams in development of new products.
* Conduct market research to establish and reaffirm product success including, pricing, positioning, performance, and packaging.
* Act as Voice of Customer in all product development decisions.
* Create detailed financial models justifying projects.

1. Brand and Market Development

* Create marketing campaigns to support the brand and lead sales performance
* Create dynamic selling tools for support of sales performance
* Work globally to develop new markets for Product Line
* Sponsor conduction of clinical trials for support of economic or outcome claims
* Build strong relationships with customers to ensure brand awareness
* Build strong relationships with competitors and other players in the field
* Provide monthly sales budgets, production demand budgets, and expense budgets
* Organize and conduct clinical training programs
* Is obsessive about brand quality

1. Organization Development
1. Develops network of experts to advance Product Line goals and objectives
2. Teaches and trains colleagues in new skills
3. Seeks feedback from peers to continuously improve
4. Acts as a Mentor when acting in a supervisory capacity

Qualifications

The successful candidate shall demonstrate:

* Proven Strategic Thinking capability, alternative analysis to a situation , and efficient resource management
* Evidence of Creativity in terms of problem solving approaches
* Grounding in Technology and practical application regarding what is and isn't feasible and under what kinds of circumstances
* Strong Technical Product & Marketing Knowledge - demonstrate strong understanding of products, customers, market/industry and competitive environment with at least 3-5 years of industry experience, including expertise in the medical device industry
* Excellent Communication and Interpersonal Skills to work effectively across organizational boundaries, with customers and sales force
* Clear Action Orientation manifested by independence, effectively balancing priorities; and timely achievement of objectives
* Drive for Success with a track record of execution, leadership, and excellence
* Team Work ability to work well with cross functional teams, global colleagues and external customers
* Comfort with Ambiguity, especially for identifying and assessing new trends and/or approaches
* Wise judgment and critical thinking skills in decision making and decision making approaches
* Proven capability to Translate Learnings/Knowledge into lasting knowledge/tools for leverage by others in future; thrives on sharing knowledge and training others

* Minimum of 3-5 years of business experience in the medical device industry with a minimum of 2 years in product and/or market management. Business experience may include marketing, sales, sales training, business development
* Bachelor's degree, MBA preferred
* Strong interpersonal and communication skills required

Job
Product Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Sr.-Product-Manager-Hypodermic-Job-NJ-07417/689718/6897186897182010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
Description

Accountable for all marketing activities supporting a Product Line within a Business Platform of the Medical Surgical Systems Business Unit. Responsible for full life cycle management of the Product Line. Actively participates in the development of the Product Line and platform global strategies. Establishes key customer relationships. develops customer requirements, and proposes new product concepts. Conducts Market Research. Acts as Voice of Customer in all decisions related to the Product Line. Supports product development activity for the extension and expansion of the Product Line and establishes claims. Launches and promotes products through conferences, literature, clinical trials, and collateral development. Responsible for managing and providing support on existing marketed products and interfacing globally with internal and external customers. Acts as owner of Product Line, ensuring maintenance of quality, regulatory, and manufacturing compliance. Establishes sales budgets. Creates marketing campaigns to drive financial performance. Benchmarks competition and stays fluent with state of the art in clinical practice. Conducts detailed analyses of the Market and Sales Performance. Crafts impactful Business Models and Marketing Plans. Presents work to Senior Leadership.

RESPONSIBILITIES

1. Strategy and Business Development

· Support development of Business Unit and Business Platform Strategy

· Identify trends in clinical practice, technology, regulatory pathways, and customer behavior.

· Source and sense new concepts and ideas.

· Benchmark competition

· Identify and conduct initial diligence on new business relationships

2. Product Development

* Define product concepts and author customer requirements.
* Lead cross-functional product development teams in development of new products.
* Conduct market research to establish and reaffirm product success including, pricing, positioning, performance, and packaging.
* Act as Voice of Customer in all product development decisions.
* Create detailed financial models justifying projects.

1. Brand and Market Development

* Create marketing campaigns to support the brand and lead sales performance
* Create dynamic selling tools for support of sales performance
* Work globally to develop new markets for Product Line
* Sponsor conduction of clinical trials for support of economic or outcome claims
* Build strong relationships with customers to ensure brand awareness
* Build strong relationships with competitors and other players in the field
* Provide monthly sales budgets, production demand budgets, and expense budgets
* Organize and conduct clinical training programs
* Is obsessive about brand quality

1. Organization Development
1. Develops network of experts to advance Product Line goals and objectives
2. Teaches and trains colleagues in new skills
3. Seeks feedback from peers to continuously improve
4. Acts as a Mentor when acting in a supervisory capacity

Qualifications

The successful candidate shall demonstrate:

* Proven Strategic Thinking capability, alternative analysis to a situation , and efficient resource management
* Evidence of Creativity in terms of problem solving approaches
* Grounding in Technology and practical application regarding what is and isn't feasible and under what kinds of circumstances
* Strong Technical Product & Marketing Knowledge - demonstrate strong understanding of products, customers, market/industry and competitive environment with at least 3-5 years of industry experience, including expertise in the medical device industry
* Excellent Communication and Interpersonal Skills to work effectively across organizational boundaries, with customers and sales force
* Clear Action Orientation manifested by independence, effectively balancing priorities; and timely achievement of objectives
* Drive for Success with a track record of execution, leadership, and excellence
* Team Work ability to work well with cross functional teams, global colleagues and external customers
* Comfort with Ambiguity, especially for identifying and assessing new trends and/or approaches
* Wise judgment and critical thinking skills in decision making and decision making approaches
* Proven capability to Translate Learnings/Knowledge into lasting knowledge/tools for leverage by others in future; thrives on sharing knowledge and training others

* Minimum of 3-5 years of business experience in the medical device industry with a minimum of 2 years in product and/or market management. Business experience may include marketing, sales, sales training, business development
* Bachelor's degree, MBA preferred
* Strong interpersonal and communication skills required

Job
Product Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Sr.-Product-Manager-Anesthesia-Job-NJ-07417/689719/6897196897192010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

Basic Job Purpose:

This individual will perform the duties of execution buying for Production and Operation requirements for the assigned productions line(s).

Principal Accountabilities:

* Develop an intimate understanding of manufactured and purchased products in one or more value streams.
* Review Purchase Order Action reports from Enterprise (ERP) system daily, ensuring that all Purchase Orders (PO's) requiring attention (new orders, push-outs, pull-ins, past due follow-up) are acted upon daily.
* Prepare PO's in accordance with the company's purchasing policies and obtain reference and confirmation numbers for all purchases.
* Review back-ordered items and outstanding PO's. Follow-up with vendors as needed to ensure on-time delivery.
* Participate in the Material Review Board and procure return material authorization information from vendors to ensure that material is dispositioned in real-time.
* Analyze and update safety stock levels as necessary according to inventory metrics.
* Work with Value Stream Planner and Procurement on supplier forecasts.
* File and track purchase history in a timely and orderly manner.
* Document and notify all appropriate areas of any backordered and/or discontinued item, as well as pro-actively work with Procurement on obsolete materials to prevent line down situations.
* Perform various inventory transactions involving manufacturing, including but not limited to the transaction of manufacturing builds and cycle count adjustments as required.
* Initiate/execute Change Orders and update Information System as required for new or updated purchased materials for the value stream.
* Serve as backup to area Planner and/or Production Coordinator as required.
* Support the Production Coordinator/Scheduler in driving cycle counting activities for the value stream transactions and ensuring records are kept in accordance with BDD-TriPath procedures and good record keeping practices.

Job Dimensions:

* Job scope will include preparing and placing PO's from approved vendors while maintaining value stream inventory targets and turns.
* Achieve line file rate goals for the value stream(s) as stipulated on an annual basis.
* This employee will be the key resource for supporting Manufacturing, Receiving, Finance, and other areas when questions arise regarding incoming shipments, items to return to vendors, and cycle counting activities.
* Key success factors for this individual will include rapid turnaround of nonconforming items, participation in Continuous Improvement Events, and identification and implementation for Lean-based pull systems. Performance will be measured against key performance indicators which may include, but are not limited to: Line Down Time %, Premium Freight ($), Cycle Count Accuracy, Material Review ($), Aging and Line Fill Rate/Back-orders (#).

Qualifications

Education and Experience Required:

* Associate's degree in Business or related field
* Minimum of 2-5 years procurement experience with previous experience in a manufacturing environment with exposure to a wide variety of commodities.
* Experience procuring components in a regulated environment such as ISO
* Experience procuring inventoried materials through an MRP system and/or other procurement and financial systems
* Proficiency with MS Office products
* Must possess the ability to work as a positive team member with a wide variety of people and disciplines within the organization as well as outside suppliers through the use of verbal, written and e-system communications

Education and Experience Preferred:

* Bachelor's degree
* Experience in procuring products for use in an FDA environment
* Exposure to or specific experience in procurement strategies such as JIT, Kanban and Lean
* For the Imaging Value Stream, previous work experience with a wide variety of commodities in a manufacturing environment including, but not limited to: sheet metals, machined metals, electronics, optical components and/or illumination systems
* CPM, ISM or APICS certification

Supervisory Responsibility:

* None

Job
Planning

Primary Location
US-North Carolina-Mebane

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/MEBANE-Procurement-Specialist-Job-NC-27302/690595/6905956905952010-04-10BDfull-timeUSDstarting0BSMebane, NC, US
Description

BD Medical - Pharmaceutical Systems has a heritage of rewarding results with more responsibility and clear accountability. Over the past decade, our business has consistently delivered double-digit growth and has a tremendous future. BD Medical -Pharmaceutical Systems, working in partnership with the pharmaceutical industry, develops an array of drug delivery systems that are critical to the integrity and delivery of medicine. Our products facilitate vaccination and therapy against disabling diseases improving the patient and caregiver's experience with medical care and protecting our families. We are proud of doing our part to further BD's mission to help all people live healthy lives.

Position Responsibilities

* Consistently improve product development processes for effectiveness and compliance
* Process owner for key R&D product development activities (DFFS and GPDS)
* Ensure quality and accuracy of integrated project plans encompassing all cross-functional activities
* Be accountable for timely delivery of all product development deliverables as specified in the plans
* Manage and provide leadership to Design and Product Development Engineers
* Ensure all interested parties have opportunities to influence and contribute to decisions and outcomes
* Create an environment in which innovation can flourish through empowerment, encouragement, and support
* Demonstrates high level of energy, intellectual curiosity, learning agility and leadership skills
* Intuitively and quickly assess people and situations and act accordingly
* Demonstrate strong and clear accountability for the group's performance and delivery
* Interface with customers to build credibility, identify technical requirements and mature our relationships

Qualifications

Education and Experience

Master in Engineering, preferably Mechanical or Biomedical and experience in product development.

7-10 years of experience in engineering, project management, and personnel management preferably in the pharmaceutical and/or medical device industry with successful track record of delivering products to market.

Knowledge and Skills

· Strong organizational leadership skills.

· Strong interpersonal and influence skills.

· Strong technical and managerial skills.

· Strong communication skills.

· Team orientation.

· Strong skills in project planning and management.

· Broad and deep understanding of disciplined product development processes, regulatory, and quality requirements.

Job
Product Design / Development

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/R-26D-Manager-Advanced-Product-Development-Job/690597/6905976905972010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

Basic Job Purpose:

This position provides technical product support and development activities towards diagnostic oncology products and/or technologies. These technologies utilize liquid based cytology and nucleic acid and protein-based biomarkers, which identify cancerous conditions, predict cancer stage or metastatic potential and monitor disease progression. The scientist applies analytical skills and knowledge to develop solutions to associated technical product challenges and verifies/validates analytical and functional performance of assay components and final product. Correlation of clinical performance to recognized standards and the successful transfer of new assay components into manufacturing are required.

Principal Accountabilities:

* Responsible for participating in the development, transfer into manufacturing, technical support, and post launch product enhancement activities of diagnostic oncology products.
* Support Quality Assurance (QA), Manufacturing, and Field Service with product troubleshooting, investigations and root cause analysis.
* Optimize, verify, and validate manufactured reagents, purchased reagents, and/or finished goods products.
* Optimize and develop Quality Control (QC) processes for reagents and assays using quantitative and/or qualitative methods.
* Perform studies to continually characterize, monitor, and/or optimize assay and reagent sensitivity and specificity.
* Participate in maintaining the design control process for product development, component verification, and product enhancement activities.
* Create feasibility studies, verification and validation protocols.
* Collect, record, report and interpret data and present results to others orally or in writing.
* Recommend adjustments to experiments/work plans in consultation with supervision.
* Perform work under moderate supervision.
* Provide technical guidance to other team members.
* Handle hazardous waste as appropriate.

Job Dimensions:

* Performance will be measured on technical capabilities in providing troubleshooting support, completeness and appropriateness of resolutions as well as thoroughness in experimental design and success of optimization and product enhancement activities.
* Metrics could involve response time, first time right, financial impact, adherence to established project plan with regard to time and budget, etc.

Qualifications

Education and Experience Required:

* BS in Biology, Molecular Biology, Biochemistry or other related field
* 2 - 5 years immunoassay development experience with proven record of success
* Proficiency in basic bioanalytical techniques (e.g SDS-PAGE, Western Blot, Enzyme assays, et. al.)
* Proven ability to participate in screening of monoclonal candidate antibodies and immunoassay development programs
* Experience with experiment design, data gathering, statistical analysis of data and interpretation of data
* Minimum of two years experience in an industrial immunoassay development setting
* Computer skills necessary to utilize commercial software packages such as data analysis, spreadsheets and word processing
* Demonstrated ability to interact and communicate effectively with multidisciplinary staff

Education and Experience Preferred:

* MS in Immunology, Molecular Biology, or Biochemistry
* Experience with Flow Cytometry
* Experience in all phases of product development
* Technical support experience in an FDA regulated environment
* Background in a clinical lab environment and/or regulated industrial setting

Supervisory Responsibility:

* None

Job
Other

Primary Location
US-North Carolina-Burlington

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BURLINGTON-Scientist-II,-Molecular-Technical-Product-Support-Job-NC-27215/692392/6923926923922010-04-10BDfull-timeUSDstarting0BSBurlington, NC, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Total Care Sales Consultant is responsible for selling the Medical Surgical Systems' product portfolio to the US acute care healthcare market segment. The portfolio includes Injection, Infusion, Surgical Blade, Scalpel, and Anesthesia product lines. The customer base is comprised of US hospitals that are 100 beds in size and larger (including facilities on hospital grounds and those that are owned by the hospital) as well as the Alternate Site.

The Total Care Sales Consultant manages his/her territory according to a FOCUS Account strategy, calling on the 20-25 hospitals that represent 70% of the territory's current volume and ADC beds. The Total Care Sales Consultant will also call on the Alternate Site market.Selling tactics include deep account penetration, broadening of departmental relationships, system selling, and use of marketing tools to communicate clinical and economic value.

Primary responsibilities include: (1) Meeting/exceeding sales budget for assigned territory; (2) managing incremental conversion opportunities from initial targeting, through evaluation, product ordering, and inservicing; (3) maintaining existing business; (4) implementing Marketing initiatives; (5) implementing national/regional contractual agreements; (6) providing routine performance reporting; (7) working collaboratively with members of MSS Regional team and across BD units with other BD field associates; (8) working with local distributor branches servicing the territory; (9) utilizing available sales support resources; and (10) exemplifying the BD core values

Territory includes Fairfield, Sacramento and Fresno.

Qualifications

Required Skills: Sales proficiency, computer proficiency (Excel, Word, PowerPoint), territory and account management

Required Degrees: Bachelors Degree

Certifications: N/A

Years of relevant work experience: a minimum of three (3) years of sales experience is required. Medical sales experience is preferred.

Travel: A minimum of 25% travel is required

Job
Field Sales

Primary Location
US-California

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Field-Sales-Consultant-Total-Care-Fairfield-Sacramento-Job-CA/693622/6936226936222010-04-10BDfull-timeUSDstarting0BSUS-California
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Laboratory Account Executive (LAE) is responsible for achieving the financial objectives of a LAE Territory, as well as assisting the region in achieving its overall sales goals by effectively implementing BD Diagnostics - TriPath's sales and marketing strategies. This individual is responsible for sales, sales forecasting, marketing feedback, best practices development, ongoing training and development, reference site development and customer satisfaction relative to sales activities.

The LAE's main responsibility is identifying and closing new business and therefore necessitates a successful proven track record of selling capital equipment as well as planning and implementing complex sales calls.

This position will be located in the Cincinnati/Columbus, OH area.

Principal Accountabilities:

1) Demonstrate efficiency and effectiveness in successful sales achievement in the LAE territory

2) Work closely with the RSM to regularly evaluate sales opportunities for BD Diagnostics - TriPath products and to ensure that territory goals/quotas for all product lines are met, if not exceeded

3) Participate on cross-functional product launch teams. Work closely with the other LAEs and Marketing Product Managers to gather best practice and centers of excellence data

4) May participate in training programs for new and existing LAEs

5) Develop and implement sales and marketing plans, including customer profiling, targeting and call schedules, to ensure achievement of all sales objectives

6) Establish realistic customer and associate expectations and then provide consistent follow-up to ensure customer and associate satisfaction meets or exceeds expectations

7) Demonstrate the ability to work with colleagues to achieve team objectives

a) Demonstrate the ability to work cooperatively with the all TriPath personnel as a member of the regional account team to achieve regional objectives through the communication of successful tactics and recommendations for continuous improvements in procedures, strategies and specific processes

b) Work with key support staff, such as the CAS and other technical support team members, to develop and implement key account evaluation plans and to update colleagues on a quarterly basis or more frequently as appropriate

c) Generate leads and sales by participating in state, regional, and national meetings as directed by the Regional Sales Manager-Laboratory Group and the Director of Sales. Activities include pre-meeting display setup if necessary; meeting support, post meeting display disassembly as needed

d) Actively participate in all training sessions and demonstrate proficiency by testing or other means as assigned at session completion

e) Identify, develop, and communicate best practices for sales and sales process that result in closed contracts and increased customer satisfaction

f) Work closely with Physician Sales Representative(s) in region to identify and close new accounts

8) Perform administrative duties with accuracy and timeliness

a) Routine weekly, monthly, and other special reports must be submitted completely and on time and must include lost business, competitive activity and other information as required by the Regional Sales Manager-Laboratory Group

b) Expenses must be documented with all receipts, submitted accurately and in a timely manner and be within company guidelines

c) Free goods/samples must be consistent with defined budgets and sent according to company policy

d) Maintain tracking policies and provide weekly updates for the territory

e) Complete all mandatory and or assigned training activities as well as any assigned development objectives

Job Dimensions

* Delivering objectives with a sense of urgency and purpose are common factors of success in this position
* Travel Requirements: varies, up to 60-70%
* Geographical Responsibility: Regional travel is required

Qualifications

Education and Experience Required:

* BA/BS in Life Sciences, Biological areas, Business or related discipline
* Five or more years experience in capital sales involving complex selling situations, with at least three years of experience in medical device sales
* Proven track record in developing new capital equipment business on a yearly basis
* Must be self motivated to succeed and have a mastery of the complex sales process
* Computer proficiency is required, including skills with the use of Microsoft Word, Excel, and PowerPoint
Posses' comprehensive knowledge of current U.S. healthcare trends that can be integrated into region sales strategies
* Candidate should have well developed organizational and time management skills
* Ideal candidates will posses the following:
* Extensive previous field experience in the sale of capital equipment/molecular diagnostics and/or IHC products in the medical marketplace
* Ability to operate independently and strategically to achieve individual and corporate goals

Education and Experience Preferred:

* Degree in Medical Technology (MT ASCP) or Microbiology
* Experience in selling laboratory products
* Proven ability to read, analyze, and interpret documents such as purchase agreements, financial reports, professional journals, package inserts, technical procedures, and government regulations
* Posses the ability to adapt to changing markets and or territory conditions while maintaining all objectives and or goals

Job
Field Sales

Primary Location
US-Ohio

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Laboratory-Account-Executive-Cincinnati-Columbus,-OH-Job-OH/693624/6936246936242010-04-10BDfull-timeUSDstarting0BSUS-Ohio
Description

The Senior Quality Engineer supports new product development and product maintenance through the application of Quality engineering skills. This person will handle multiple projects and tasks, from product inception through product launch and maintenance. Additionally, they will play an active role in the processes to ensure products meet quality standards consistent with both Corporate and unit policies, while meeting all design control and other regulatory requirements and will represent Quality on project teams for both Design and Manufacturing. This role also supports plant activities in process validation, process capability issues and customer issues, initiates corrective and preventive action, with an eye to increased capability and customer satisfaction and supports Quality System implementation.

Qualifications

* Minimum Bachelor's Degree in Engineering is required.
* 5-7 years experience in Quality Engineering is required.
* A minimum of 10 years engineering experience in the medical device or pharmaceutical industry is desirable.
* Certified Quality Engineer (CQE), Certified Quality Auditor (CQA) and/or Regulatory Assurance Certification (RAC) or Six Sigma certification are desirable.

Job
Quality Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Sr.-Quality-Engineer-Job-NJ-07417/693627/6936276936272010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

General Function: The Sales Associate position is an entry level position for Sales openings within BDMedical Surgical Systems. The candidate must have a sales aptitude even if their previous work experience is limited. The Sales Associate will report directly to the reporting Regional Business Manager and will be assigned responsibility for an open sales territory. The Sales Associate will earn quarterly compensation based on their development and improvement in specific skill based criteria. The role is a one year assignment with the expectation that upon completion they will receive a "Good" review and be promoted to a Sales Consultant earning commission based on the performance of the territory.

Responsibilities
The Sales Associate will be responsible for completing the assigned training activities to support their growth. They will also be asked to validate customer engagement through regular updates of Brand in Use and the SF1 contact database

Qualifications

Bachelor's degree is required and the candidate must have an aptitude for sales. The candidate must be highly motivated; goals oriented and have a demonstrated work ethic.

Highly desirable attributes

The preferred candidate will have a minimum of one year applicable experience following completion of their academic requirements. Additionally, the ideal candidate would have a college history reflective of academic excellence accompanied by a balance of extracurricular activities. The candidate should be able to demonstrate a drive for success as an individual and in team situations. The candidate should also have demonstrated computer skills to support our administrative and financial proficiency goals. The ideal candidate would also have some exposure in the development of a clinical skill set through coursework or life experience.

Only local candidates will be considered (Jacksonville, Tallahassee or Valdosta) for this position.

Job
Sales Representative / Account Management

Primary Location
US-Florida

Other Locations
US-Georgia

Shift
Rotating

Relocation Available
No]]>http://www.bd-careers.com/job/Field-Sales-Associate-Primary-Care-North-Florida-South-Georgia-Job-FL/693628/6936286936282010-04-10BDfull-timeUSDstarting0BSGeorgia, FLORIDA OTHER LOCATIONS US, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

Basic Job Purpose: Responsible for manufacturing and assembly of one or more clinical and commercial medical devices. Follows detailed work instructions and maintains records to comply with regulatory requirements, Good Manufacturing Practices (GMP), and Standard Operating Procedures. May assist with in process testing to ensure instruments meet specifications.

Principal Accountabilities:

* Maintain manufacturing documentation and reconciliation of paperwork as required for GMP.
* Complete scheduled production runs in an efficient, timely manner as required by manager.
* Keep Instrument Lead and higher level technician(s) informed of any changes or problems with production assemblies (i.e. out of stock items, back ordered items, production equipment problems.)
* Interact with Value Stream Planner and Procurement Specialist in performing periodic cycle counts and assist in to resolving inventory discrepancies.
* Interface with Value Stream and Quality team on the initiation of Change Orders (CO) and Material Action Reviews (MAR) processes.
* Comply with training in all manufacturing areas.
* Perform other duties as required to meet the needs of the department and company.
* May provide guidance and training to lower level technicians.
* Handle hazardous waste as appropriate.

Job Dimensions:

* Works on assignments that are routine to semi-routine in nature where ability to recognize deviation from accepted practice is required.
* Performs assembly tasks involving aligning, fitting, and adjustment of components and subassemblies, which require special care in handling.
* Extensive use drawings, diagrams, or blueprints as a reference source for performing assembly tasks with minimum supervision.
* Normally receives general instructions on routine work, detailed instructions and training on new assignments.
* Contributor to achieving Value Stream Key Performance Indicators:

Safety: Days lost to accident

Quality: DHR error & QC rejects

Delivery: Daily production

Cost Delivery: Material variance vs. Build

Productivity: Hours per Instrument

* Follow detailed standard work instructions to assemble a variety of components of exacting tolerances into sub-assemblies, units or systems.
* Use hand and power tools to perform tests, assemble components, and secure panels, wire harnesses, in addition to miscellaneous assembly operations as indicated in work instructions
* Perform incidental electrical/electronic assembly work
* Perform troubleshooting and rework activities on instruments that do not meet operating parameters as described in work instructions.

Qualifications

Education and Experience REQUIRED:

* High School diploma or equivalent
* 2-4 years assembling electro-mechanical instruments/equipment or successful completion of Instrument Manufacturing Technician I - Trainee level
* Experience and training in electronics and trouble electromechanical medical instruments
* Exposure to an FDA or other federally regulated environment

EDUCATION AND EXPERIENCE PREFERRED:

* Associates degree in electronics
* Assembly of computer hardware and loading of software in Windows XP environment

Job
Manufacturing

Primary Location
US-North Carolina-Mebane

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/MEBANE-Manufacturing-Technician-II-Instruments-Job-NC-27302/694218/6942186942182010-04-10BDfull-timeUSDstarting0BSMebane, NC, US
Description

Required to work within a team developing a molecular diagnostic assay for an instrument platform capable of extracting nucleic acids from biological specimens. Reporting to the Group Leader, the successful candidate will be responsible for optimization of the assay chemistry and sample processing procedures, together with the design and execution of appropriate analytical verification and validation studies.

DUTIES AND Responsibilities:


1. Apply broad-based knowledge and experience in molecular biology to meet specific objectives and solve problems.
2. Under moderate supervision, design and execute experiments as well as analyze and interpret results, optimize assay conditions, and/or troubleshoot problems.
3. Collect, record, report and present results to peers and supervisor/manager either orally or in writing.
4. Understand and leverage published research in molecular diagnostics.
5. Interact with other R&D (Research and Development) scientists to solve problems and provide support to other functional groups.
6. Draft documentation associated with manufacturing of reagents, test protocols, and standard operating procedures.

Qualifications

MINIMUM Qualifications:


KNOWLEDGE AND SKILLS:

* Proficiency in a broad range of techniques in molecular biology including nucleic acid isolation, hybridization-based detection, and real-time PCR . Experience in the design and optimization of PCR systems and with automated liquid handling systems is desirable.
* A history of self-motivation and work within a team environment is essential.
* Experience in processing of infectious biological samples for the recovery of nucleic acids, together with a strong background in microbiology, virology and /or clinical laboratory science is advantageous.
* Knowledge of Current Good Manufacturing Practices and product development are desirable.
* Excellent verbal and written communication skills are necessary.

EDUCATION AND EXPERIENCE:

* Bachelor's or Master's Degree in Life Sciences
* Minimum of 2 years of laboratory experience in molecular biology.

Job
Product Design / Development

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Associate-Scientist-Scientist-Molecular-Job-MD-21201/694220/6942206942202010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
Description

BD Medical - Pharmaceutical Systems has a heritage of rewarding results with more responsibility and clear accountability. Over the past decade, our business has consistently delivered double-digit growth and has a tremendous future. BD Medical -Pharmaceutical Systems, working in partnership with the pharmaceutical industry, develops an array of drug delivery systems that are critical to the integrity and delivery of medicine. Our products facilitate vaccination and therapy against disabling diseases improving the patient and caregiver's experience with medical care and protecting our families. We are proud of doing our part to further BD's mission to help all people live healthy lives.

Position Responsibilities

* Implements the strategic vision for R&D to their organization
* Accountable for product development from concept to market launch to meet business objectives.
* Ensure quality and accuracy of integrated project plans encompassing all cross-functional activities. Engage in detailed review of cross-functional plans and be accountable for their success.
* Align dedicated and shared resources cross-functionally to optimize and ensure success of new product development.
* Product development management: Perform periodic reviews of progress against plans. Ensure plans are executed appropriately within department. Be accountable for timely delivery of all product development deliverables as specified in the plans
* Effectively select, develop, organize, motivate, and mentor staff. Organize and develop effective and efficient product development teams.
* Develop detailed budgets in accordance with project and department plans, and business objectives. Manage budget diligently and be accountable to perform to the budget.
* Maintain an overview of state-of-the-art technology development within the related business. Effectively leverage technical experts in addressing technical issues, providing technical direction, and advising on technical capabilities and mix of staff.
* Participate in the evaluation and assessment of competitive products, processes or new trends that could impact our business.
* Organize and communicate to ensure efficient and effective transition from research to development to manufacturing.
* Contract and partnership management: Identify best-in-class industry product development partners and establish business relationships. Ensure quality and accuracy of integrated project plans encompassing all contract and partnership activities. Engage in detailed review of these plans and be accountable for their success.
* Ensure appropriate processes are followed for effective and timely engagement of other parts of the company in product development activities.
* Ensure compliance with BD quality policies, procedures, and practices through appropriate communication, training, and education of sound quality assurance principles.
* Ensure compliance with all local, state, federal, and BD safety regulations, policies, and procedures.

Qualifications

Education and Experience

Master in Engineering, preferably Mechanical or Biomedical and experience in product development.

Minimum of 7-10 years of experience in engineering, project management, and personnel management preferably in the pharmaceutical and/or medical device industry with successful track record of delivering products to market.

Knowledge and Skills

· Strong organizational leadership skills.

· Strong interpersonal and influence skills.

· Strong technical and managerial skills.

· Strong communication skills.

· Team orientation.

· Strong skills in project planning and management.

· Broad and deep understanding of disciplined product development processes, regulatory, and quality requirements.

Job
Product Design / Development

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/R-26D-Manager-Product-Engineering-Job/694221/6942216942212010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
Description

Incumbent will function as a project manager and technical resource for a wide variety of distribution operational issues with three North American Distribution Centers. Key activities include, but not limited to: space planning, warehouse layout, productivity measurement, pallet stacking patterns, product packaging & codification and material flow. Incumbent will be responsible for overall management/maintenance protocol of Mechanized Conveyor and Sortation system at BD's Plainfield Distribution Center.

Additionally, incumbent will have responsibility for managing operations material handling equipment maintenance schedule along with developing and managing a replacement strategy. Responsibilities include evaluating and recommending work processes and work streams to determine opportunities for improving operational efficiencies. Incumbent will be responsible for managing Labor Management Systems across network and identifying focus areas for process improvements. LMS standards and time study validation process are required to insure current labor model and productivity measures are current.

Candidate will function as key project manager in the design and implementation new Distribution Center and/or integrating new business requirements into the network. Additionally, the incumbent will lead sustainability efforts across the 3 DC Network identifying opportunities to reduce carbon foot print, recycle, reduce waste, etc in support of driving towards achieving LEED status.

Incumbent will interface with 3 Party Logistics Provider leadership team, DC Management, BD Plants and Business Units, Vendors, Suppliers, Consultants and other Supply Chain Functions to achieve best fit solutions.

Qualifications

5 to 7 years Distribution or Logistics Engineer experience.

B.S. Engineering, Operations Research or Logistics

Able to travel

Customer Service and results driven.

Job
Logistics / Distribution / Customs

Primary Location
US-Indiana

Other Locations
US-California-Redlands, US-New Jersey-Trenton

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Distribution-Engineer-Job-IN/696612/6966126966122010-04-10BDfull-timeUSDstarting0BSTrenton, NJ, US
Description

As a Senior Polymer Engineer your knowledge of materials and creative ideas will directly improve product performance for high volume disposable medical devices that are used in millions of medical procedures worldwide, making a real difference in improving healthcare, changing medical practice, and saving lives.

BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 29,000 associates in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public.

· BD focuses strategically on achieving growth in three worldwide business segments: BD Medical, BD Diagnostics and BD Biosciences:

BD Medical is among the world's leading suppliers of medical devices and the leading innovator in injection- and infusion-based drug delivery since 1906, when BD built the first-ever facility in the U.S. to manufacture needles and syringes.

BD Diagnostics is a leading provider of products for the safe collection and transport of diagnostic specimens, as well as instruments and reagent systems to accurately detect a broad range of infectious diseases, healthcare-associated infections and cancers.

BD Biosciences is a world leader in bringing innovative diagnostic and research tools to life scientists, clinical researchers, laboratory professionals and clinicians who are involved in basic research, drug discovery and development, biopharmaceutical production and disease management.

· Revenues rose to $7.156 billion for the fiscal year ended September 30, 2008. BD generates over 50 percent of its revenues outside the United States.

· In FY2008, BD invested $396 million in research and development.

· BD was founded as a partnership in 1897, incorporated in 1906. BD became a publicly held company in 1962. The stock is traded on the New York Stock Exchange with the symbol BDX.

· BD employs approximately 28,000 associates worldwide in 184 locations in nearly 50 countries.

* This position is located in Sandy, UT (suburb of Salt Lake City, UT and home of the 2002 Winter Olympics)
* Activities in the Sandy area: skiing, hiking, rock climbing, fishing, mountain biking, snowmobiling, golfing, and running amidst spectacular scenery
Come see why Sandy, UT is the place to be: http://www.sandy.utah.gov/

Qualifications

Education

BS degree (MS preferred) in polymer engineering or materials science/engineering with at least 6 years of relevant experience, preferably in medical devices.

Experience

·
· Determining optimum polymers given design constraints such as chemical compatibility, biocompatibility, aging, sterilization, radiation, stresses, creep, manufacturing processes, regulatory compliance, and environmental impact.

· Direct experience with polyurethanes, polycarbonates, silicones, and epoxies.

· High-volume manufacturing and assembly processes, particularly those of plastic injection molding, metal stamping, packaging, and automated assembly techniques, including solvent bonding, adhesive bonding, ultrasonic welding, and interference-fitting

· Directly applying DOE, statistical methods, GD&T, and tolerancing
Contact and non-contact metrology

Skills

* Careful, deliberate, disciplined, meticulous, and well organized in documenting plans, requirements, drawings, design reviews, and test methods
* Excellent interpersonal, communication and influencing skills working with an expanded core team including marketing, quality, regulatory, and manufacturing personnel
* Strong understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions
* Proven ability to quickly learn new subject matter
* Drive and self-motivation for product and process improvement

Knowledge

Knowledge of disciplined product development processes, regulatory and quality requirements such as 21CFR820.30

Responsibilities

·
· Collaborating with cross-functional teams to engineer robust and manufacturable design solutions throughout the lifetime of our global products

· Lead the evaluation of competitive products as well as new trends related to materials.

· Provide technical direction for existing and new products regarding material design, synthesis, identification, formulation, selection, qualification, and characterization.

· Developing and executing project plans with timely deliverables

· Designing experiments to verify, validate, and implement recommended materials solutions

· Deriving engineering requirements related to material properties from user needs and intended uses.

· Engineering support activities related to Supplier qualification

· Gaining visibility by presenting and conducting project design reviews

· Leveraging personal creativity to contribute to the BD intellectual property knowledgebase
Train and mentor junior associates

Job
Materials Engineering

Primary Location
US-Utah-Sandy

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/SANDY-Senior-Polymer-Engineer-(PVA-Platform)-Job-UT-84070/696613/6966136966132010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
Description

As a Senior Product Engineer your ideas will directly improve product performance for high volume disposable medical devices that are used in millions of medical procedures worldwide, making a real difference in improving healthcare, changing medical practice, and saving lives.

BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 29,000 associates in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public.

· BD focuses strategically on achieving growth in three worldwide business segments: BD Medical, BD Diagnostics and BD Biosciences:

BD Medical is among the world's leading suppliers of medical devices and the leading innovator in injection- and infusion-based drug delivery since 1906, when BD built the first-ever facility in the U.S. to manufacture needles and syringes.

BD Diagnostics is a leading provider of products for the safe collection and transport of diagnostic specimens, as well as instruments and reagent systems to accurately detect a broad range of infectious diseases, healthcare-associated infections and cancers.

BD Biosciences is a world leader in bringing innovative diagnostic and research tools to life scientists, clinical researchers, laboratory professionals and clinicians who are involved in basic research, drug discovery and development, biopharmaceutical production and disease management.

· Revenues rose to $7.156 billion for the fiscal year ended September 30, 2008. BD generates over 50 percent of its revenues outside the United States.

· In FY2008, BD invested $396 million in research and development.

· BD was founded as a partnership in 1897, incorporated in 1906. BD became a publicly held company in 1962. The stock is traded on the New York Stock Exchange with the symbol BDX.

· BD employs approximately 28,000 associates worldwide in 184 locations in nearly 50 countries.

* This position is located in Sandy, UT (suburb of Salt Lake City, UT and home of the 2002 Winter Olympics)
* Activities in the Sandy area: skiing, hiking, rock climbing, fishing, mountain biking, snowmobiling, golfing, and running amidst spectacular scenery
Come see why Sandy, UT is the place to be: http://www.sandy.utah.gov/

Qualifications

Education

BS degree (MS preferred) in Mechanical Engineering or MS Industrial Engineering with at least 6 years of relevant experience, preferably in medical devices.

Experience

· Developing CAD models (SOLIDWORKS Preferred)

· Model and analyze design solutions with FEA (Abaqus preferred)

· Designing production equivalent rapid-prototypes

· High-volume manufacturing and assembly processes, particularly those of plastic injection molding, metal stamping, packaging, and automated assembly techniques, including solvent bonding, adhesive bonding, ultrasonic welding, and interference-fitting

· Directly applying DOE, statistical methods, GD&T, and tolerancing

· Contact and non-contact metrology

· Hands-on experience building parts with lathe, end-mill, and other standard shop equipment

Skills

* Careful, deliberate, disciplined, meticulous, and well organized in documenting plans, requirements, drawings, design reviews, and test methods
* Excellent interpersonal, communication and influencing skills working with an expanded core team including marketing, quality, regulatory, and manufacturing personnel

· Strong understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions
Proven ability to quickly learn new subject matter

Knowledge

Knowledge of disciplined product development processes, regulatory and quality requirements such as 21CFR820.30

Responsibilities

· Collaborating with cross-functional teams to engineer robust and manufacturable design solutions throughout the lifetime of our global products

· Enhancing performance, quality, and cost of existing products by refining product requirements and applying DF(x) while relying on exemplary knowledge of engineering fundamentals

· Strategizing and executing project plans with timely deliverables

· Administering test methods, including fixture design, method development, measurement system analysis, and safe laboratory implementation

· Designing experiments to verify, validate, and implement recommended design solutions

· Deriving engineering requirements from user needs and intended uses.

· Developing design verification traceability matrices and associated requirements analysis.

· Engineering support activities related to Supplier qualification.

Generating detailed technical reports, engineering drawings, and bills of materials to document

Job
Mechanical Engineering

Primary Location
US-Utah-Sandy

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/SANDY-Sr.-Product-Engineer-(IVA-Nexiva-Platform)-Job-UT-84070/696614/6966146966142010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
Description

As a Senior Product Engineer your ideas will directly improve product performance for high volume disposable medical devices that are used in millions of medical procedures worldwide, making a real difference in improving healthcare, changing medical practice, and saving lives.

BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 29,000 associates in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public.

· BD focuses strategically on achieving growth in three worldwide business segments: BD Medical, BD Diagnostics and BD Biosciences:

BD Medical is among the world's leading suppliers of medical devices and the leading innovator in injection- and infusion-based drug delivery since 1906, when BD built the first-ever facility in the U.S. to manufacture needles and syringes.

BD Diagnostics is a leading provider of products for the safe collection and transport of diagnostic specimens, as well as instruments and reagent systems to accurately detect a broad range of infectious diseases, healthcare-associated infections and cancers.

BD Biosciences is a world leader in bringing innovative diagnostic and research tools to life scientists, clinical researchers, laboratory professionals and clinicians who are involved in basic research, drug discovery and development, biopharmaceutical production and disease management.

· Revenues rose to $7.156 billion for the fiscal year ended September 30, 2008. BD generates over 50 percent of its revenues outside the United States.

· In FY2008, BD invested $396 million in research and development.

· BD was founded as a partnership in 1897, incorporated in 1906. BD became a publicly held company in 1962. The stock is traded on the New York Stock Exchange with the symbol BDX.

· BD employs approximately 28,000 associates worldwide in 184 locations in nearly 50 countries.

* This position is located in Sandy, UT (suburb of Salt Lake City, UT and home of the 2002 Winter Olympics)
* Activities in the Sandy area: skiing, hiking, rock climbing, fishing, mountain biking, snowmobiling, golfing, and running amidst spectacular scenery
Come see why Sandy, UT is the place to be: http://www.sandy.utah.gov/

Qualifications

Education

BS degree (MS preferred) in Mechanical Engineering or MS Industrial Engineering with at least 6 years of relevant experience, preferably in medical devices.

Experience

· Developing CAD models (SOLIDWORKS Preferred)

· Model and analyze design solutions with FEA (Abaqus preferred)

· Designing production equivalent rapid-prototypes

· High-volume manufacturing and assembly processes, particularly those of plastic injection molding, metal stamping, packaging, and automated assembly techniques, including solvent bonding, adhesive bonding, ultrasonic welding, and interference-fitting

· Directly applying DOE, statistical methods, GD&T, and tolerancing

· Contact and non-contact metrology

· Hands-on experience building parts with lathe, end-mill, and other standard shop equipment

Skills

* Careful, deliberate, disciplined, meticulous, and well organized in documenting plans, requirements, drawings, design reviews, and test methods
* Excellent interpersonal, communication and influencing skills working with an expanded core team including marketing, quality, regulatory, and manufacturing personnel

· Strong understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions
Proven ability to quickly learn new subject matter

Knowledge

Knowledge of disciplined product development processes, regulatory and quality requirements such as 21CFR820.30

Responsibilities

· Collaborating with cross-functional teams to engineer robust and manufacturable design solutions throughout the lifetime of our global products

· Enhancing performance, quality, and cost of existing products by refining product requirements and applying DF(x) while relying on exemplary knowledge of engineering fundamentals

· Strategizing and executing project plans with timely deliverables

· Administering test methods, including fixture design, method development, measurement system analysis, and safe laboratory implementation

· Designing experiments to verify, validate, and implement recommended design solutions

· Deriving engineering requirements from user needs and intended uses.

· Developing design verification traceability matrices and associated requirements analysis.

· Engineering support activities related to Supplier qualification.

Generating detailed technical reports, engineering drawings, and bills of materials to document

Job
Mechanical Engineering

Primary Location
US-Utah-Sandy

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/SANDY-Sr.-Product-Engineer-(IVA-Nexiva-Platform)-Job-UT-84070/696615/6966156966152010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
Description

As a Senior Product Engineer your ideas will directly improve product performance for high volume disposable medical devices that are used in millions of medical procedures worldwide, making a real difference in improving healthcare, changing medical practice, and saving lives.

BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 29,000 associates in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public.

· BD focuses strategically on achieving growth in three worldwide business segments: BD Medical, BD Diagnostics and BD Biosciences:

BD Medical is among the world's leading suppliers of medical devices and the leading innovator in injection- and infusion-based drug delivery since 1906, when BD built the first-ever facility in the U.S. to manufacture needles and syringes.

BD Diagnostics is a leading provider of products for the safe collection and transport of diagnostic specimens, as well as instruments and reagent systems to accurately detect a broad range of infectious diseases, healthcare-associated infections and cancers.

BD Biosciences is a world leader in bringing innovative diagnostic and research tools to life scientists, clinical researchers, laboratory professionals and clinicians who are involved in basic research, drug discovery and development, biopharmaceutical production and disease management.

· Revenues rose to $7.156 billion for the fiscal year ended September 30, 2008. BD generates over 50 percent of its revenues outside the United States.

· In FY2008, BD invested $396 million in research and development.

· BD was founded as a partnership in 1897, incorporated in 1906. BD became a publicly held company in 1962. The stock is traded on the New York Stock Exchange with the symbol BDX.

· BD employs approximately 28,000 associates worldwide in 184 locations in nearly 50 countries.

* This position is located in Sandy, UT (suburb of Salt Lake City, UT and home of the 2002 Winter Olympics)
* Activities in the Sandy area: skiing, hiking, rock climbing, fishing, mountain biking, snowmobiling, golfing, and running amidst spectacular scenery
Come see why Sandy, UT is the place to be: http://www.sandy.utah.gov/

Qualifications

Education

BS degree (MS preferred) in Mechanical Engineering or MS Industrial Engineering with at least 6 years of relevant experience, preferably in medical devices.

Experience

· Developing CAD models (SOLIDWORKS Preferred)

· Model and analyze design solutions with FEA (Abaqus preferred)

· Designing production equivalent rapid-prototypes

· High-volume manufacturing and assembly processes, particularly those of plastic injection molding, metal stamping, packaging, and automated assembly techniques, including solvent bonding, adhesive bonding, ultrasonic welding, and interference-fitting

· Directly applying DOE, statistical methods, GD&T, and tolerancing

· Contact and non-contact metrology

· Hands-on experience building parts with lathe, end-mill, and other standard shop equipment

Skills

* Careful, deliberate, disciplined, meticulous, and well organized in documenting plans, requirements, drawings, design reviews, and test methods
* Excellent interpersonal, communication and influencing skills working with an expanded core team including marketing, quality, regulatory, and manufacturing personnel

· Strong understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions
Proven ability to quickly learn new subject matter

Knowledge

Knowledge of disciplined product development processes, regulatory and quality requirements such as 21CFR820.30

Responsibilities

· Collaborating with cross-functional teams to engineer robust and manufacturable design solutions throughout the lifetime of our global products

· Enhancing performance, quality, and cost of existing products by refining product requirements and applying DF(x) while relying on exemplary knowledge of engineering fundamentals

· Strategizing and executing project plans with timely deliverables

· Administering test methods, including fixture design, method development, measurement system analysis, and safe laboratory implementation

· Designing experiments to verify, validate, and implement recommended design solutions

· Deriving engineering requirements from user needs and intended uses.

· Developing design verification traceability matrices and associated requirements analysis.

· Engineering support activities related to Supplier qualification.

Generating detailed technical reports, engineering drawings, and bills of materials to document

Job
Mechanical Engineering

Primary Location
US-Utah-Sandy

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/SANDY-Sr.-Product-Engineer-(PVA-Platform)-Job-UT-84070/696618/6966186966182010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
Description

GENERAL FUNCTION

The Global Marketing Manager is responsible for the strategic and financial performance of their respective product families through comprehensive and timely Marketing and Product strategy development and execution.

RESPONSIBILITIES

* Participate in the development of and execute marketing and product strategies to achieve or exceed the business unit objectives of innovation and growth for the Market Segment portfolio. This will include analyzing market and customer information, identifying new product innovations, optimizing product portfolio, launching new products and line extensions, managing product lifecycles, forecasting, pricing strategies and guidelines, etc.
* Define and execute product strategy, multi-generational product roadmaps, development priorities, and release planning that meets or exceeds customer expectations.
* Participate in the development of and executes worldwide marketing plans, including: phase IV clinical study planning, advertising and promotion, sales tools, public relations, public policy, seminars, etc.
* Develops a global sales and marketing plan (SMAP) that defines market development, marketing activities, promotional strategies, and related sales objectives.
* Develops thorough competitive intelligence and market analysis in support of competitive strategies; proposes and executes competitive strategies.
* Support the Global Product Development System (GPDS) process as a core team member (CTM) and is accountable for completion of respective marketing deliverables, if assigned. Includes driving market-related initiatives through communications and collaborative efforts with all levels of other functional areas represented on project teams (e.g., R&D, Regulatory Affairs, Clinical and Scientific Affairs, etc.)
* Effectively partner and collaborate with regional marketing leaders, R&D, Clinical and Scientific Affairs, Business Development and other functions to ensure development and execution of comprehensive marketing and product strategy.
* Adhere to all company policies, procedures and business ethics codes and ensures that they are communicated and implemented within the team.

Qualifications

* BS/BA in business or science is required. MBA desirable.
* A minimum of 4 years of relevant marketing experience in medical device, clinical diagnostics and/or pharmaceutical industry is required with a consistent track-record of high performance and results. Sales experience desirable.
* Experience working globally is preferred.
* Proficienty in MS Office applications is required.

SPECIAL SKILLS

* Track record of achievement in delivering projects and influencing business outcomes.
* Strategic thinker with demonstrated ability to help formulate and implement marketing and product strategies, convert these into tactical marketing plans, and deliver results.
* Solid business acumen and knowledge of clinical and/or laboratory market environment.
* Sound decision making capabilities and the ability to make decisions, even in absence of consensus when necessary.
* Creative out-of-the-box thinker who is intellectually curious, stays current on new trends, and takes calculated risks with novel ideas.
* Excellent presentation and communication skills for a wide variety of audiences.
* Excellent interpersonal skills, and ability to develop strong relationships with key opinion leaders, customers, advisory boards, and potential or existing business partners.
* Managerial courage to speak up when important information or questions must be raised and takes action when issues must be addressed.
* Ability to influence across and up the organization to effectively negotiate and persuade others.
* Ability to work effectively on diverse, cross-functional teams.
* Strong organizational skills and ability to meet tight deadlines in an environment of competing priorities. Ability to routinely work on multiple tasks with multiple people while effectively prioritizing.
* Flexibility to travel globally to regions and customer sites at least 30% of the time.

Job
Product Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Global-Marketing-Manager,-Preanalytical-Systems-Job-NJ-07417/696621/6966216966212010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
Description

GENERAL FUNCTION

The Global Marketing Manager is responsible for the strategic and financial performance of their respective product families through comprehensive and timely Marketing and Product strategy development and execution.

RESPONSIBILITIES

* Participate in the development of and execute marketing and product strategies to achieve or exceed the business unit objectives of innovation and growth for the Market Segment portfolio. This will include analyzing market and customer information, identifying new product innovations, optimizing product portfolio, launching new products and line extensions, managing product lifecycles, forecasting, pricing strategies and guidelines, etc.
* Define and execute product strategy, multi-generational product roadmaps, development priorities, and release planning that meets or exceeds customer expectations.
* Participate in the development of and executes worldwide marketing plans, including: phase IV clinical study planning, advertising and promotion, sales tools, public relations, public policy, seminars, etc.
* Develops a global sales and marketing plan (SMAP) that defines market development, marketing activities, promotional strategies, and related sales objectives.
* Develops thorough competitive intelligence and market analysis in support of competitive strategies; proposes and executes competitive strategies.
* Support the Global Product Development System (GPDS) process as a core team member (CTM) and is accountable for completion of respective marketing deliverables, if assigned. Includes driving market-related initiatives through communications and collaborative efforts with all levels of other functional areas represented on project teams (e.g., R&D, Regulatory Affairs, Clinical and Scientific Affairs, etc.)
* Effectively partner and collaborate with regional marketing leaders, R&D, Clinical and Scientific Affairs, Business Development and other functions to ensure development and execution of comprehensive marketing and product strategy.
* Adhere to all company policies, procedures and business ethics codes and ensures that they are communicated and implemented within the team.

Qualifications

* BS/BA in business or science is required. MBA desirable.
* A minimum of 4 years of relevant marketing experience in medical device, clinical diagnostics and/or pharmaceutical industry is required with a consistent track-record of high performance and results. Sales experience desirable.
* Experience working globally is preferred.
* Proficienty in MS Office applications is required.

SPECIAL SKILLS

* Track record of achievement in delivering projects and influencing business outcomes.
* Strategic thinker with demonstrated ability to help formulate and implement marketing and product strategies, convert these into tactical marketing plans, and deliver results.
* Solid business acumen and knowledge of clinical and/or laboratory market environment.
* Sound decision making capabilities and the ability to make decisions, even in absence of consensus when necessary.
* Creative out-of-the-box thinker who is intellectually curious, stays current on new trends, and takes calculated risks with novel ideas.
* Excellent presentation and communication skills for a wide variety of audiences.
* Excellent interpersonal skills, and ability to develop strong relationships with key opinion leaders, customers, advisory boards, and potential or existing business partners.
* Managerial courage to speak up when important information or questions must be raised and takes action when issues must be addressed.
* Ability to influence across and up the organization to effectively negotiate and persuade others.
* Ability to work effectively on diverse, cross-functional teams.
* Strong organizational skills and ability to meet tight deadlines in an environment of competing priorities. Ability to routinely work on multiple tasks with multiple people while effectively prioritizing.
* Flexibility to travel globally to regions and customer sites at least 30% of the time.

Job
Product Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Global-Marketing-Manager,-Preanalytical-Systems-Job-NJ-07417/696622/6966226966222010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD Biosciences, a segment of BD, is one of the world's leading businesses focused on bringing innovative research and clinical tools to life scientists and clinicians. Its product lines include: flow cytometers; cell imaging systems; monoclonal antibodies; research reagents; diagnostics assays; and tools to help grow tissue and cells.

BD is an EEO/AA employer

About us

Description

JOB SUMMARY

Responsible for providing field-based advanced applications specialist support for BD Cell Analysis products -- with emphasis on the clinical market segment -- serving as a technical resource for BD Cell Analysis sales and other field associates and BD Cell Analysis customers. Uses technical expertise in clinical applications to support BD Cell Analysis reagent and instrument customers, in alignment with BD business initiatives. Serve as a technical resource for in-house departments. Works independently without direct supervision. This position is a field based position and ideally will be located in the Southwestern United States.

DUTIES AND RESPONSIBILITIES

Provide on-site / electronic technical consultation to BD customers on BD Cell Analysis clinical workflow (products, instruments, software, reagents, analytical approach). Record customer contact information and interests; provide that information to in-house resources as necessary.

Provide on-site / electronic technical consultation with BD Sales Associates on any of the BD Cell Analysis clinical workflow. Maintain high level of expertise in instruments, reagents and software and applications, and develop expertise on new products.

Assist with BD Sales with instrument and reagent set demonstrations in workshop form, or as a bona fide product demonstration.

Assist with multicolor panel / assay development, which may include support for clinical validation. Provide feedback into Marketing to make adjustments to assays where necessary and required.

Perform assay and instrument problem troubleshooting consultation to customers, on-site or by phone. Provide support for clinical laboratory certification investigations as are prudent and necessary. Provide information the Field Service on instrument status. Report on problems to appropriate in-house resource. Follow-up to track resolution of issues.

Identify significant clinical trends or new issues of strategic importance and communicates them to BD field or in-house resources as appropriate. Participate in product incident report/customer complaint reporting systems. Contribute to design changes through request for change process. Provide formal and informal feedback and recommendations throughout BD Cell Analysis. Make recommendations for new products and applications and enhancements for existing products. Contribute to the product development process by serving on Commercial Excellence and other committees.

Provide on-site support for sales/marketing events, including technical support for trade shows, Marketing sponsored seminar series, and users' meetings.

Perform hands-on customer workshops for instruments and assay systems. Assist customers with clinical workflow development, optimization and implementation.

Develop and deliver technical presentations. Consult with Marketing and Sales to develop product promotional materials in alignment with BD business initiatives.

Consult with the Validation Lab. Assist with periodic in-house validations. Collaborate with Validation staff to write, execute and report on validation protocols.

Keeps abreast of the basic requirements for compliance in own area of work and complies with those requirements. Participate as required in training on regulatory issues affecting own area of work. Bring regulatory compliance questions/issues to the attention of management.

Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participate in Environmental Health and Safety programs. Address corrective actions whenever a hazard is identified. Notify supervisor of all observed hazardous conditions or unsafe work practices.

Travel for on-site support approximately 70%. Maintain reasonable travel budget in alignment with BD practices.

Perform other related duties and assignments as required.

Qualifications

Qualifications:


A minimum of a Bachelor's degree

A minimum of 5 years clinical flow cytometry experience

Ability to travel a minimum of 70% of the time

A valid driver's license.

Assets:


Experience in flow cytometric cell sorting applications highly desired.

Individuals with a degree in clinical / life science fields preferred.

Previous experience with BD Cell Analysis clinical workflow is highly desired.

Previous experience providing onsite technical customer support

Previous technical demonstration experience in support of Sales.

Thorough knowledge of Pharmingen and BDIS products.

Effective analytical, troubleshooting, and problem solving skills.

Effective interpersonal, written and oral communication skills.

Effective organization and planning skills.

Job
Technical / Field Service

Primary Location
US-Texas

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/Technical-Applications-Specialist-Job-TX/698388/6983886983882010-04-10BDfull-timeUSDstarting0BSUS-Texas
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Principal Engineer, R&D, Materials Technology will be part of a cross-functional product development team working to develop new drug delivery products to meet current unmet customer and clinical needs. This person will be responsible for product development activities from concept generation, prototyping, and design verification to product launch. This person will also be the key individual leading Finite Element Modeling and simulation to integrate material properties and product design and relate them to functional performance. The ideal candidate will have a passion for product development and solving complex technical problems. He/She should also be able to reduce complex principles into simple language for effective communication across all functions and levels of the organization to enable effective decision making.

Qualifications

Requirements include:

Minimum of 5 years experience plus MS or 3 years experience plus PhD in a R&D organization within the medical device industry.

Experience with CAD software, such as SolidWorks, Cosmos, ABAQUS, ANSYS, FLUENT etc.

Expertise in computational modeling and design, finite element analysis and simulation

Knowledge of design control procedures, including experience with Design History File (DHF), Design Verification (DV), IQ/OQ/PQ

Prior experience working with ISO/USP/EP and other standards for medical devices.
Knowledge of polymers and materials is preferred

Job
Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/Principal-Engineer-R-26D,-Materials-Technology-Job/699206/6992066992062010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 29,000 associates in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public.

•BD employs approximately 28,000 associates worldwide in 184 locations in nearly 50 countries.

About us

Description

We are recruiting an R&D Principal / Staff Engineer who will be supporting our Environmental Sustainability Initiative.

In this position, you will be responsible for leading cross-business initiatives concerning new technology development efforts for BD's next generation medical devices. Working in a cross-functional environment, you will provide senior leadership, advanced engineering skills, and project management skills to identify, plan, break down and solve complex problems, and provide technical direction to others. Using these advanced technical skills, you will conceive, plan and lead technical development activities from concept through successful commercialization. You will develop an in-depth assessment of relevant next-generation technologies and products, and lead the evaluation and assessment of competitive products, processes or new trends, identifying gaps and opportunities. You will lead the project support of R&D IP strategy and processes and participate in a work environment that prizes scientific inquiry and basic fundamental first principles.

Qualifications

Master's Degree (PhD strongly preferred) in technical field, such as mechanical engineering, materials science and engineering, biomedical engineering, or closely related fields with a minimum of 8+ years of experience.

Minimum of 8+ years experience in engineering, preferably in the medical device and/or pharmaceutical industry with successful track record of delivering products to market or developing commercially viable technology.

Experience with disciplined product development processes and regulatory and quality requirements.

Comprehensive knowledge of environmental science principles and ecological impacts.
In-depth experience in at least one environmental sub-field is preferred, such as: design for environment, carbon accounting, life cycle assessment, sustainable materials, waste management, etc.

Team player with proven ability to deliver results.

Ability to reduce complex technical issues into easy to understand language and communicate effectively to a cross-functional team.
Passion for product development and solving deep technical problems

Job
Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Staff-Engineer-Job-NJ-07417/699207/6992076992072010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

Design medical devices that optimally address customer needs and create impact globally. Identify unmet and underserved needs through deep customer engagement, interfacing and ethnography. Drive a global leader in medical devices to produce ergonomic products that delight users and improve patient outcomes. Influence BD to become ever more customer facing.

Qualifications

BS, BFA or Masters in Industrial Design/Design Engineering

* 2-4 years of experience, preferably in medical device industry.
* Proficiency in 3D CAD. SolidWorks strongly preferred
* Inspiring 2D skills via sketching, Illustrator, Photoshop, etc.
Knowledge of injection molded plastic part design/decoration
Proven Mechanical aptitude, ability to deliver design data to engineering, manufacturing, etc.
* Knowledge of prototyping and manufacturing processes
* Aptitude in form development
Experience in ethnography a plus
* Experience in user interface design is a plus
* Excellent verbal and visual/graphical communication skills
Desire and ability to get customer input for improving and innovating products
* Ability to work collaboratively in multi disciplinary teams
* Able to handle multiple tasks and projects at the same time
* A self-managing, motivated and entrepreneurial nature
*
Research, design and develop medical device products as a member of the design team.

*
Leads customer needs identification in medical clinical settings and identifies novel concepts that uniquely address customer needs, enabling BD to win in competitive markets.

*
Develop customer relationships with organizations and conduct primary market research that will enable validation/invalidation of early product concepts

*
Engage in all aspects of product development from concept through testing and development to commercialization, with an emphasis on customer research, product usability, concept generation, and design detailing.

*
Represent R&D on multidisciplinary product development teams and provide technical competency in the area of Industrial Design and or Design Engineering.

*
Ability to synthesize multiple, ambiguous, often contradictory inputs to obtain clarity regarding customer and market dynamics.
Some travel required
*
Team player with proven ability to deliver results.

Ability to reduce complex clinical needs and settings to a basic understanding.

Ability to drive design and development with a business, market and strategic focus that will result in significant top line revenue growth.
Passion for uncovering customer needs, determining how to best address those needs and global, medical device product development.

Job
Industrial Engineering

Primary Location
US-Utah-Sandy

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/SANDY-Principal-Engineer-Job-UT-84070/699208/6992086992082010-04-10BDfull-timeUSDstarting0BSSandy, UT, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Assists with research and development in collaboration with others on research projects or work assignments. Accountable for effectively executing moderately complex experiments within a defined framework. May perform troubleshooting when necessary. Makes detailed observations, analyzes data and interprets results with minimal guidance in routine tasks. Prepares technical reports, summaries and quantitative analyses of assigned research projects. Works on problems of diverse scope where analysis of situations or data requires evaluation of various factors. Exercises judgment within generally defined procedures and practices in selecting methods and techniques for obtaining results. May provide guidance to lower level personnel within the department.

Qualifications

Qualifications

* Requires a minimum of a Bachelors of Science degree
* A minimum of 3 years experience in a research and development laboratory environment.
* A minimum of 2 years immunoassay development experience.
* A minimum of 1 year experience in an FDA or ISO regulated environment.

Assets

* Flow Cytometry experience is a plus.
* Ability to perform complex tasks with minimum supervision
* Demonstrated experience completing work assignments against aggressive deadlines.
* Knowledge of Microsoft Excel and Microsoft Word.
* The ideal candidate will have quantitative data analysis skills, attention to detail and technical adeptness.
* Effective written and verbal communication skills are necessary.
* Ability to trouble-shoot problems ranging from simple to moderate complexity is necessary.
* Experience successfully collaborating with multiple groups and functions is highly desired.

Job
Life Sciences R & D

Primary Location
US-California-San Jose

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-JOSE-Reagent-Dev-Associate-III-Job-CA-95101/699209/6992096992092010-04-10BDfull-timeUSDstarting0BSSan Jose, CA, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

A Metallurgist/Materials Engineer is sought for a medical device technology development program. This role is an opportunity to apply a fundamental scientific approach towards development of products that are central to company growth strategies.

The primary responsibilities for this position are:

* To identify, assess and conduct metallurgical technology development activities to process metallic devices
* To gain insight into the metallurgical requirements of materials and develop a detailed scientific understanding of all aspects of related metallurgical and manufacturing processes.
* To conduct microstructural, mechanical and topographical characterization of the processed materials using optical and electron microscopy as well as analysis of composition and texture.
* To interface with manufacturing sites and quality assurance personnel for trouble shooting and technology transfer.
To support the team leader with regard to project proposals, management, execution of tasks and preparation of status reports.

Qualifications

A PhD in metallurgical/materials engineering from a top research institution is required, but candidates with a Masters degree and several years of relevant experience would also be considered.

Demonstrable metallurgical and microstructural characterization expertise is required, especially for stainless steels.

Excellent communication and presentation skills are required to interact with customers, production personnel, marketing and research scientists/engineers

Familiarity with one or more of the following metallurgical processes is preferred and will be regarded very favorably: Laser/TIG welding, wire/tube drawing, heat-treating, grinding and electrochemical finishing.

Job
Materials Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Metallurgist-Materials-Engineer-Job-NJ-07417/699211/6992116992112010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines.
•BD focuses strategically on achieving growth in three worldwide business segments: BD Medical, BD Diagnostics and BD Biosciences:

•In FY2008, BD invested $396 million in research and development.

•BD was founded as a partnership in 1897, incorporated in 1906. BD became a publicly held company in 1962. The stock is traded on the New York Stock Exchange with the symbol BDX.

•BD employs approximately 28,000 associates worldwide in 184 locations in nearly 50 countries.

About us

Description

We are recruiting an R&D Principal Engineer who will be supporting our Environmental Sustainability Initiative.

In this position, you will be responsible for leading cross-business initiatives concerning new technology development efforts for BD's next generation medical devices. Working in a cross-functional environment, you will provide senior leadership, advanced engineering skills, and project management skills to identify, plan, break down and solve complex problems, and provide technical direction to others. Using these advanced technical skills, you will conceive, plan and lead technical development activities from concept through successful commercialization. You will develop an in-depth assessment of relevant next-generation technologies and products, and lead the evaluation and assessment of competitive products, processes or new trends, identifying gaps and opportunities. You will lead the project support of R&D IP strategy and processes and participate in a work environment that prizes scientific inquiry and basic fundamental first principles.

Qualifications

Master's Degree (PhD strongly preferred) in technical field, such as mechanical engineering, materials science and engineering, biomedical engineering, or closely related fields with a minimum of 5+ years of experience.

Minimum of 5+ years experience in engineering, preferably in the medical device and/or pharmaceutical industry with successful track record of delivering products to market or developing commercially viable technology.

Experience with disciplined product development processes and regulatory and quality requirements.

Comprehensive knowledge of environmental science principles and ecological impacts.

In-depth experience in at least one environmental sub-field is preferred, such as: design for environment, carbon accounting, life cycle assessment, sustainable materials, waste management, etc.

Team player with proven ability to deliver results.

Ability to reduce complex technical issues into easy to understand language and communicate effectively to a cross-functional team.
Passion for product development and solving deep technical problems

Job
Mechanical Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Principal-Engineer-Job-NJ-07417/699212/6992126992122010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

BD Medical Surgical Systems is searching for a Principal Engineer to work within the Hypodermic business R&D. As a Principal Engineer, the ideal candidate will lead the design and development efforts for disposable medical devices for high volume manufacturing. This person will be capable of identifying and breaking down complex technical problems resulting in robust solutions. This person will plan, lead and execute cross functional projects from concept to manufacturing including advanced product development, support of continuous improvement projects, capacity expansion efforts and development and launch of product line extensions. Additionally, the candidate will be expected to actively participate in the development of new technologies which will help meet current and future clinical unmet needs. As a world leader in the development of drug delivery systems, we are seeking an innovative candidate with a demonstrated ability to work directly with customers, identifying unmet needs and organizing a cross functional core team that will drive development to launch.

Qualifications

MS degree in Mechanical Engineering with at least 5 years of relevant experience.

· Experienced in planning, leading and executing product development projects within a cross functional team environment

· Demonstrated technical leadership achieving business critical goals

· Obtaining and managing customer needs

· Experience with technical product design for high volume manufacture

· Setting cross functional priorities to achieve scheduled milestone completion

Effective communication cross functionally and within business leadership

· Experience in computational modeling, Finite Element Analysis and simulation

· Practical experience utilizing Design for Six Sigma tools and methodologies

Knowledge of good manufacturing practice within the medical device industry preferred

· Experience in phase gated product development process preferred

· Knowledge of Medical device regulations and practices

· Knowledge of polymer properties and selection
Ability to identify, break down and solve complex technical problems

Job
Mechanical Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Principal-Engineer-Job-NJ-07417/699213/6992136992132010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

BD is a world leader in the design/engineering and development of medical devices. The Needle Technology Product Development Engineer will be responsible for design and development of the device/patient interface in drug delivery systems used worldwide.

The Needle Technology Product Development Engineer will: support requirements and change management (product and process) for existing products; design and develop new cannula/needle products; design, develop and qualify measurement systems for key product features; identify and utilize modeling, simulation and visualization techniques required for analysis and design; innovate in product technology, design and performance measurement; plan and lead R&D activities within cross functional team.

Qualifications

Masters in Mechanical Engineering or related field; PhD preferred

Minimum of 5 years experience (for Masters) or 3 years experience (for PhD) in the medical device industry in R&D.

CAD/Parametric modeling software (Solidworks); foundation in Solid Mechanics and FEA; measurement system design/development; technical writing and presentation

Design controls, verification, validation; requirements management; voice of customer.

Passion for product development and solving deep technical problems

Job
Mechanical Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Principal-Engineer-Job-NJ-07417/699214/6992146992142010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

Lead an R & D team from the definition phase through global product launch of a game changing combination medical device.

Qualifications

Masters in Mechanical Engineering/Chemical Engineering/Pharmaceutical Engineering or related field with at least 5 years of relevant experience, and/or PhD degree with at least 3 years of experience.

* Minimum of 5 years experience (for MS) or 3 years experience (for PhD) in the medical device industry in R&D.
* Demonstrated ability to lead a technical team in the development and commercialization of a medical device through a Pre-Market Approval (PMA) regulatory pathway, including translation of customer requirements into product requirements and specifications for a combination drug-device.
* Demonstrated ability to provide all necessary experimental design, testing, product development and transfer to large scale manufacturing for a combination drug-device.

Skills

• Excellent interpersonal, communication and influencing skills

• Strong technical judgment

• Experienced in project planning

• Demonstrated leadership.

• Understanding of disciplined product development processes, regulatory and quality requirements

• Results driven and action oriented

Understanding of and experience with, pharmaceutical test method development for safety, efficacy and

stability.

Ability to develop and validate test methods

Effectively lead and direct the work of other engineers and laboratory technicians to achieve objectives

* Identify, break down and solve complex problems, and provide technical direction to others
* Independently plan and execute to achieve design and development objectives
* Set priorities for self and team
* Participate as a member of a cross-functional team or lead a cross-functional team to deliver to business-critical product development commitments
* Using expert technical skills, conceive, plan and lead development activities from concept through successful commercialization
* Leverage understanding of first engineering principles, advanced engineering methods, data and judgment to influence the course of product development activities
* Participate in implementation of technology transfer from research to development to manufacturing.
* Ensure appropriate processes are followed for effective and timely engagement of related parties in completion of designated project activities.
* Develop understanding of customer needs and processes to ensure relevant and innovative product development solutions.
* Actively seek training to improve skills. Ensure technical lessons are reviewed, learned, and disseminated. Actively teach and promote learning.
* Ensure compliance with BD quality policies, procedures and practices as well as with all local, state, federal and BD safety regulations, policies and procedures.
* Team leader with proven ability to deliver results.
* Knowledge of pharmaceutical stability and packaging.
* Experience with combination drug-device manufacture.
* Ability to plan multiple work-flows and identify ways to optimize time lines and reduce technical development risk.
* Ability to reduce complex technical requirements and analysis into easy to understand language and communicate effectively to a cross-functional team.

Passion for leading technical product development, commercialization and launch.

Job
Mechanical Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Principal-Engineer-Job-NJ-07417/699215/6992156992152010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

Lead a completely cross-functional (R & D, Regulatory, Medical, Manufacturing, Operations) team from the definition phase through global product launch of a game changing combination medical device.

Qualifications

Masters in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Mechanical Engineering, Pharmaceutical: Chemistry, Science or Management or related field; PhD preferred

Minimum of 7 years experience (for MS) or 5 years experience (for PhD) in the medical device industry in R&D.

Demonstrated ability to lead a team in the commercialization of a medical device through an IDE submission to Pre-Market Approval (PMA).
The successful candidate will have an advanced understanding of disciplined product development processes and regulatory and quality requirements in medical device and combination product development.

Understanding of pharmaceutical development, experience with clinical trials development, regulatory pathway planning and execution, and combination drug-device development and commercialization.

Team leader with proven ability to deliver results.

Knowledge of pharmaceutical stability and packaging.

Ability to plan multiple work-flows and identify ways to optimize time lines and reduce development risk.

Ability to reduce complex cross-functional requirements into easy to understand language and communicate effectively to a cross-functional team.

Passion for leading product development, commercialization and launch.

Job
Mechanical Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Staff-Engineer-Job-NJ-07417/699216/6992166992162010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

Identify and quantify world-wide current markets and trends to identify significant, new, growth opportunities in global medical device manufacturing. Support business development (acquisition analysis, partnership analysis, etc.) to validate or in-validate investment theses. Provide broad, cross-functional, business analytics to optimize business understanding and business function globally in developed and emerging markets.

Qualifications

Bachelors in Business Administration or Economics, or Masters in Engineering or other technical discipline with strong interest in business.

* Minimum of 2 years experience for major management consulting firm (preferably with exposure to the healthcare industry)
* Must have used deep analytical analysis to uncover truths and opportunities (for improvement, for growth, etc.) for business function optimization.

* Financial Models, Financial analysis, market segmentation.

* Demonstrated, strong analytic/math capabilities a must.Ability to reduce complex spaces to fundamentals and to identify and synthesize reliable and current information sources into a comprehensive and accurate understanding of business reality.
* Ability to synthesize multiple, ambiguous, often contradictory inputs to obtain clarity regarding customer and market dynamics.
*
Team player with proven ability to deliver results.

Ability to reduce complex and ambiguous market dynamics into easy to understand, fundamental concepts and communicate effectively across functions.
Passion for healthcare and deep analytical insight.

Job
Product Research

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Analyst-Job-NJ-07417/699217/6992176992172010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

As a member of the Bedford Plant operations team, provides process support towards attaining plant goals and objectives in the area of quality, cost improvements, safety and waste. Support plant New Product Development (NPD) team on transfer of new products to the manufacturing environment. Responsible for identifying and improving critical processes for better, faster and lower cost production. Investigate and trouble shoot technical problems and offer solution to resolve problem areas. Determine best utilization of equipment, facilities, material and personnel flow. Initiates and participate in various continuous improvement projects for Operational Excellence. Will exercise judgment and obtain cross functional support in developing manufacturing methods, techniques, and evaluation criteria for obtaining results.

Qualifications

Requires a Bachelor's Degree in an Engineering discipline with minimum 5 years of experience in all aspects of the production processes within a laboratory environment; or equivalent combination of education and experience. Life Sciences experience preferred

Basic knowledge of statistics and certification as a six sigma green belt

Familiarity with process validation and design of experiments is desirable

Experience must include fiscal responsibility and/or accountability for multi-disciplined scientific activity in an industrial or commercial setting.

ISO, GMP & SAP experience strongly preferred; Experience in Continuous Improvement (Lean Manufacturing, Six Sigma & Validations) strongly preferred.

Equal Opportunity Employer

Job
Manufacturing

Primary Location
US-Massachusetts-Bedford

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BEDFORD-Process-Engineer-Bedford-Job-MA-01730/701130/7011307011302010-04-10BDfull-timeUSDstarting0BSBedford, MA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The senior core team leader is responsible for leading the cross functional core team, and its extended team members, of large complex new to market product development programs. Scope includes new major initiatives or major product development programs within a business unit or across multiple business units.

The Senior Core Team Leader leads the team in executing all aspects of major product development projects including successful product development over the complete product life cycle (inception through development, high volume manufacturing, post launch and commercialization). The Senior Core Team Leader is ultimately responsible for the execution, quality and results of his or her project and the success of the resulting product in the market. The Senior Core Team Leader is responsible for the creation of the project work breakdown structures, integrated business plans and product requirements. He/She manages day-to-day activities of team members, tracks progress against plan, manages the project budget, identifies project risks and provides plans to mitigate those risks. The Core Team Leader should be capable of managing varying degrees of program and project size, cost, complexity or risk.

The Senior Core Team Leader is responsible and accountable to lead and direct cross-functional activities and outcomes including:

· Leading large complex new to market product development programs or new major initiatives within a business unit or across multiple business units

· Planning resource requirements and negotiating team resource assignments with functional managers within a business and/ or across business units

· Leading the creation of the cross-functional project plan, including budget and resource planning, to fulfill the product concept.

· Aligning and managing all cross-functional activities to deliver the product on time and on budget per contract while meeting all agreed upon technical, operational, business and customer requirements.

· Negotiate, resolve personal/team conflicts and project/functional conflicts., and drive consensus among team members to accomplish project and business goals

· Defining, refining, and understanding customer requirements.

· Successfully track progress to requirements, plan and resolve deviations

· Architecting or refining the high-level product concept to fulfill the customer requirements.

· Providing work definition and direction to the assigned cross-functional Core Team Members.

· Providing coaching and mentoring to Core Team members and providing significant feedback to functional leaders regarding training needs of, and resources required by, the core team.

· Providing meaningful and significant input to the performance of core team members that is fully considered in their year-end performance reviews and compensation recommendations.

· Successful commercial, design, and business project reviews; makes PDT aware of, and proposes solutions to, unanticipated or potential issues/concerns as soon as they are known.

· Successful product design.

· Superior product quality in the field.

· Product acceptability by intended customers; spends time with customers/end-users and constantly invests in understanding customer environment.

· Successful product commercialization.

· Completion of accurate and timely reporting, e.g. project portfolio server (G3), resource allocation, dashboard updates.

· Contributes to the continuous improvement in organization's ability to execute programs and projects from initiation through launch.

· Coaching and mentoring new Core Team Leaders.

Qualifications

* BSME and at least a Masters in ME. MBA or PhD preferred.
* 10 + years successful project & program management experience with new and complex medical devices
* PMI training
* Has successful launched multiple new medical device products from concept through launch
* 15 + years medical device product development and high volume manufacturing experience
* Experience developing Class III medical devices
* Has managed or overseen complex clinical trials with Class III devices, experience with drug/device combination products a plus
* Experience with biological medical fluids and polymers a plus
* Must be a skilled and determined communicator and negotiator
* Must have strong leadership skills and be very relationship and collaborative oriented

Knowledge of specific procedures/practices

* Product Development Phase gate Processes and Procedures
* Quality System Regulations for Medical Devices
* Technology Development Process
* Product Development Performance Metrics
* Preliminary and Integrated Business Plans
* DFSS/DFMA
* Post Launch Reviews
* Voice of Customer Methodologies
* Team Formation and Dynamics
* Project Management

Job
Product Design / Development

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/Sr.-Core-Team-Leader-R-26D-Platform-Job/701132/7011327011322010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
Description

The Clinical Education Specialist for the Medical/Surgical Unit will be the BD expert in vascular access. This individual will lead the clinical education program for the organization ensuring that the field sales team is kept up to date with vascular access best practice. In addition, this role supports the sales team in customer facing activities, providing clinical support throughout the entire sales cycle.

Along with providing clinically essential educational programs, this individual will be responsible for buidling relationships with key opinion leaders, organizations and institutions as well as presenting at major conferences.

Qualifications

* Registered Nurse with advanced vascular access skills
* Minimum 5 years experience in vascular access
* Expertise in program development and delivery
* Exceptional presentation skills
* Strong interpersonal and problem-solving skills
* Experience in a business environment would be an asset

Job
Other

Primary Location
CA-Ontario-Oakville

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/ONTARIO-CDN-CLINICAL-EDUCATION-SPECIALIST-Job-CA-91710/702138/7021387021382010-04-10BDfull-timeUSDstarting0BSOakville, ONTARIO, CA
Description

Within the context of a professional practice, Code of Ethics, and the established vision and values of the organization, the incumbent works closely with the Clinical Specialist for Sales and Training, BIC Coordinator and Regional Sales Reps to deliver safety product in-services to nurses (RNs) and other hospital disciplines.

Uses knowledge of clinical practice, change management and adult learning principles to ensure effective provision of training, and coaching.

Collaborates with the BD Sales Reps, Patient Care Managers and Educators to coordinate activities, promote continuous quality improvement, and resolution of issues.

This is a casual, contract role which would be suited for former, retired or part-time nurses, or those with flexible schedules.

Consultants will be engaged on a per project basis in their region.

Qualifications

EDUCATION & EXPERIENCE

Experience and proficiency with IV insertion or infusion therapy a benefit.

Experience across various types of hospital clinical departments with some teaching, mentoring, orientating or preceptorship experience

KNOWLEDGE & ABILITIES

Broad knowledge of clinical practices in infusion and injection therapies, hospital policies and procedures.

Comprehensive knowledge of the standards for nursing practice (CRNBC, CRMB, CARNA), and/or laboratory standards in their Province/Territory. Familiarity with Standards of IV Practice (CVAA, INS)

Understanding of principles of adult education and change management.

Candidates will have proven organization and problem solving skills and the ability to work independently.

Preference will be given to those candidates with diverse and experienced clinical background (such as RN, LPN, BN, RT, MLT or Paramedic).

Job
Other

Primary Location
Canada

Other Locations
CA-Manitoba, CA-Saskatchewan, CA-Alberta-Edmonton, CA-Alberta, CA-Manitoba-Winnipeg, CA-British Columbia-Vancouover, CA-Saskatchewan-Regina, CA-Alberta-Calgary, CA-British Columbia, CA-Yukon, CA-Northwest Territories

Shift
Rotating

Relocation Available
No]]>http://www.bd-careers.com/job/NORTHWEST-TERRITORIES,-YUKON-CDN-MEDSURG-INSERVICE-CONSULTANT-WEST-Job-NORT/702139/7021397021392010-04-10BDfull-timeUSDstarting0BSNorthwest Territories, YUKON, CA, Ca
Description

The Team Leader, Distribution will be responsible for ensuring that the BD Canada Oakville, Distribution Center operates in the most efficient and effective manner. The role is responsible for all aspects of the DC operation including Inventory Control as well as having a dotted line responsibility for security and facilities. This role will work with the Manager Distribution to develop and implement strategies that will improve our service offering to the customer and drive cost savings. The Team Leader, Distribution will have a significant role in the development of associates, budget management and contribute to the performance of the Operations organization as a whole.

· Warehouse operations management - utilizing the Distribution Supervisor, supervise the daily activities of D.C associates. Activities to include pick, pack, loading, shipping, and replenishment.

· Resource management - optimum utilization of space, capacity management, and dotted line responsibility for all facets of facilities. Work with the Manager Distribution to optimize labour.

· Channel partner relations/Customers - understanding of customer, segment or channel specific requirements. Able to partner with customers and develop win win solutions.

· Reverse logistics- ensure strict adherence to the returns policy for recalls and PIRs working in conjunction with Quality and Regulatory. Timely receiving and processing of returns and financial reconciliation.

· Physical inventory control - proactive and reactive cycle counting, responsible to post monthly inventory metrics. Adjustments and financial reconciliation for over, shorts and damaged product. Inventory location slotting to determine best location for product.

· Batch, serialisation and expiration management - inventory management of short dated product. First in first out and instrument serialization.

· Product and waste disposal - disposition of distressed, expired, recalled, and returned inventory and packaging.

· Continuous improvement - deploy Lean Six Sigma driving improved performance through a fully deployed measurement system and utilization of benchmarking.

· People leadership - lead direct reports by training, coaching, performing performance evaluations, creating development and succession plans.

· Budget and financial performance - responsible for departmental budgeting and management of the budget throughout the year.

· Regulatory and quality compliance - ensure that policies and procedures are documented, up to date and deployed.

· Regulations - work with other Team Leaders and Lead Hands to ensure compliance with all Transportation, Customs, Health Canada and other regulations along with all customer requirements.

· Equipment management - determination of the need for and the efficient use of equipment in the warehouse and ensure an active preventive maintenance program is in place.

· Technology - understand and keep up to date on technology that will improve service, ensure that quality requirements are met and reduce cost. Includes ERP, WMS systems warehouse technologies.

· Strong data analytical ability. Able to produce and interpret data to support fact based decision making.

Qualifications

POSITION REQUIREMENTS:

· University degree required.

· 3-5 years D.C. management experience with a focus in order fulfillment, pick-pack, quality and inventory control.

Skills and Competencies:

· Strategic and tactical planning

· Working knowledge of Transportation, Import, Export and Supply Chain Planning.

· Business acumen

· Analytical

· Managing, leading and developing people

· Influencing others

· Process effectiveness

· Interpersonal skills

· Multi task and ability to prioritize

· Action oriented and drive for results

· Teamwork

· Proficient in Excel/Word/PowerPoint.

Job
Other

Primary Location
CA-Ontario-Oakville

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/ONTARIO-CDN-TEAM-LEAD,-DISTRIBUTION-Job-CA-91710/702143/7021437021432010-04-10BDfull-timeUSDstarting0BSOakville, ONTARIO, CA
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Works within standards and operating procedures to plan, perform, and make decision regarding the set up and operations of a variety of production equipment, including automated machine processes and controls to perform routine assembly-line production functions of filling, packing, assembling, labeling and inspecting. Uses independent judgment in troubleshooting and problem solving under general supervision. May perform clean up functions in areas. Analyzes and evaluates charts, follows simple diagrams, testing, and inspecting procedures. Maintains accurate records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization). Effectively works in a team setting, supporting team goals and objectives. Make effective decisions relative to position requirements. Responsible for accurate inventory control. Strong emphasis on Continuous Improvement (shift start up meetings, Kaizen Action sheets, etc.).

Qualifications

* Must be able to read, write, analyze/evaluate charts, follow simple diagrams and perform basic arithmetic.
* Must be able to maintain continuous mental & visual attention (hand-eye coordination).
* Must be able to lift and/or move items on a routine basis throughout the day of up to 25 pounds.
* Minimum 6 months manufacturing experience and High school diploma or equivalent is required.
* Basic proficiency with PCs (Personal Computers) and basic use of a Windows environment is required.

Job
Production

Primary Location
US-Maryland-Baltimore

Shift
Second Shift / Afternoon Start

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORESHIFTSECOND-SHIFT-Production-Operator-II-Job/702144/7021447021442010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
Description

Summary:

The Infection Prevention Consultant reports to the Worldwide Director of Infection Prevention and is responsible for these key areas:

* Primary focus will be the provision of expert-level domain expertise in Infection Prevention, Infection Control and Healthcare Acquired Infection management as it relates to the sales process and enhancing customers' ability to obtain maximum benefit from BD Information Management solutions post-implementation.
* Support BD sales associates in communicating the value of BD Informatics solutions to multiple levels within a healthcare institution. Contribute as part of a multi-functional team to implement a portfolio selling approach and describe the value of systems integration with other BD product lines.
* Establish and maintain customer relationships to ensure customer delight with BD solutions, acting as a consultant to customers in order to enhance the scope, sophistication and effective use of BD solutions in setting priorities for their Infection Prevention and HAI management program.
* Provide continuing customer value through ongoing communication activities related to implementation of domain best practices as it relates to purchased platforms.
* Contribute to internal and external documentation resources in support of the BD informatics solutions.
* Contribute domain expertise to cross-functional teams involved in the new product development process.

Sales Pathway Support

* With BD Sales Specialists, drive and support sales of BD Informatics solutions in the identified market segment and across business units. Utilize available resources that include sales, technical services, and marketing to meet sales and business goals.
* Provide expert-level domain expertise in Infection Prevention, Infection Control and Healthcare Acquired Infection management during sales calls, including conference calls, live web demonstrations, live onsite demonstrations and technical presentations.
* With sales associates, communicate the value of BD Informatics solutions as part of an integrated solution to multiple levels within a healthcare institution from Infection Preventionist to institution executives.
* With BD technical associates, coordinate requirements gathering meetings to audit customer processes and capabilities, identify and document customer needs, and propose appropriate solutions that will meet the defined needs.
* Communicate the value of systems integration with other BD product lines.
* Provide support at trade shows and BD sponsored workshops as required.

Customer Implementation Support

* Provide appropriate guidance to the BD technical team to ensure a complete and effective implementation process, ensuring key customer learning and priorities are communicated.
* Manage seamless transition from selling process to the BD implementation team with handover at project kickoff meetings.

Account Maintenance

* Establish and maintain customer relationships to unsure customer delight with BD solutions, and maximize account retention.
* As part of account management responsibilities, consultant to customers in order to enhance their sophistication and degree of adoption and utilization of BD solutions in Infection Prevention and HAI Management.
* Provide continuing customer value through ongoing communication activities related to implementation of domain best practices as it relates to purchased platforms.
* Identify at-risk customers, or where processes or capabilities are sub-optimal, and work with sales and service functions to deliver advanced solutions.
* Provide continuing customer value through ongoing communication activities related to implementation of domain best practices as it relates to purchased platforms.

Administrative/Miscellaneous

* Contribute domain expertise to cross-functional teams involved in the new product development process, including requirements definition and prototype review.
* Monitoring of software evaluations, including protocol adherence, monitoring, end point data analysis, and outcome presentation.
* Manage administrative accountabilities as assigned, e.g. monitoring expenses to budget, timely reporting and updates to administrative systems, and competitive intelligence data.

Travel

*
Field-based assignment operating from a home-office, with approximate 75% west regional travel expectation.

Qualifications

Knowledge/Skills:

* Extensive experience in a clinical healthcare setting, successfully delivering infection control, infection prevention and healthcare acquired infection management programs.
* Experience in professional organizations, as evidenced by publications, presentations etc. preferred
* Proven ability to influence peers in best practices related to Infection Prevention, Surveillance and HAI management practices
* Demonstrated effective interpersonal skills/customer facing skills; including effective internal and external communications, presentation skills and knowledge transfer ability.
* Superior verbal and written communication skills (presentations experience a plus).
* Passion for providing superior service, with demonstrated aptitude for customer facing skills, crisis/conflict resolution and ability to establish strong professional relationships.
* Works well in a team environment with demonstrated ability to coordinate multiple functions to a successful objective.
* Demonstrated success in project management, with a track record in achieving and delivering against key objectives and timelines.
* Comfortable balancing many projects at once.
* Able to work at a fast pace with minimal supervision or structure.
* Demonstrated aptitude and interest in computers and technology and the ability to patiently communicate abstract concepts.
* Demonstrated knowledge and proficient use of various computer and software systems is required, including email, internet, and office productivity packages.
* Demonstrated ability to solve problems through investigation, deduction and logical reasoning is expected.
* Demonstrated analytical and process thinking skills required. Capable of analyzing all relevant factors in a complex cause and effect system, and make appropriate decisions.
* An understanding of typical laboratory workflow activities is desired.

Education:

* B.S. / B.A. degree required (Nursing, Infection Control, Medical Technologist)
* Certified Infection Control (CIC) or minimum master's degree in related healthcare profession.

Experience:

* Minimum 3 years relevant experience in Infection Control, Infection Prevention, Infectious Disease.
* Leadership in professional organizations as evidenced by publications, presentations etc. preferred.
* 2+ years experience in a customer-facing role in the health care industry highly desired.
* Sales experience an advantage.

Job
Sales Representative / Account Management

Primary Location
United States

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/UNITED-STATES-Infection-Prevention-Consultant-West-Job/702150/7021507021502010-04-10BDfull-timeUSDstarting0BSUnited States
Description

Sales Associate, North Western Ontario, BD Medical Systems

Job Group: 3

Reports to: Regional Business Manager, BD Medical Surgical Systems, Eastern Canada

GENERAL FUNCTION:

The Sales Associate is responsible for the field sales success in North Western Ontario Working with the Regional Business Manager, the Sales Associate will be responsible for developing and implementing annual sales strategies designed to meet the Medical business' over all sales and strategic objectives with focus on execution of our Patient Safety and Healthcare Worker Safety strategies.

KEY Responsibilities:


* Achieve sales goals by establishing sales targets in line with budget expectations
* Work closely with Marketing and Clinical Teams in implementing our strategic objectives around providing comprehensive solutions for our customers, and evaluating new market opportunities to ensure continued growth and profitability.
* Utilize the tools and principals of the blue sheeting/Miller Heiman account planning tools to ensure proper account management of key initiatives.
* Continued development of the relationships and business partnership with the COHPA group of hospitals
* Responsible for the expense budget of the territory

Qualifications

Qualifications:


* Minimum of 3 years sales experience in Acute Care setting, with consistent track record of high performance
* University degree in Business and/or Sciences
* Extensive interpersonal skills, must be team-focused
* Must be customer focused and possess a good understanding of current customer needs
* Ability to build and maintain effective working relationships with both internal & external customers.
* Self-motivated team-player
* Strong analytical and negotiating skills
* Demonstrated time management and prioritization skills
* Working knowledge of Microsoft Office & Lotus Notes

Job
Sales Representative / Account Management

Primary Location
CA-Ontario

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/CA-ONTARIO-Sales-Associate,-Northwestern-Ontario-Job/702152/7021527021522010-04-10BDfull-timeUSDstarting0BSCA-Ontario
About BD

BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

About us

Description

Responsible for the critical launch activities associated with the instrumented product platforms in the assigned sales region. Continues to identify new sales opportunities and to develop strong relationships with key stakeholders. Develops sales opportunities with targeted and segmented accounts. Travels extensively within assigned region (30+% of time). Acts as an expert on instrumented platforms at a technical, operational, logistical and financial level.

DUTIES AND Responsibilities:


* Identifies and works with key customer, thought leaders,target accounts to achieve regional sales objectives/budget.
* Attains or exceeds overall sales plan for both realized and new business dollars.
* Focuses on developing processes through field activity that will result in critical information gathering and tiered account strategy.
* Total responsibility for all assigned instrumented accounts; competitive conversions, driving and closing business.
* Engages in site/account visits focusing on gaining customer commitment to instrumented platforms and closing business.
* Maintains schedules and time lines for product activities. Drives closure of identified key initiatives.
* Communicates product learnings/knowledge and successful sales strategies.
* Responsible for utilizing Sales and Marketing tools and programs to ensure consistent value positioning across platforms and to meet/exceed goals and objectives.
* Responsible for utilizing available internal resources to meet/exceed sales objectives.
* Demonstrates Account and Territory Management.
* Is the 'expert' on assigned instrumented platforms. Thoroughly understands and is able to communicate to the customer and others technical, operational, logistical and financial aspects.

Qualifications

MINIMUM Qualifications:


KNOWLEDGE AND SKILLS:

Sales Skills: Exemplifies early adopter behaviors - absorbs and applied technical information; skilled technical sales professional. Relationship builder with thought leaders and customers. Capably grows technical knowledge base through such relationships and provides solutions and unshakeable alliances. Demonstrates expertise in technical, operational, logistical, and financial aspects of the instrumented platform business.

Sales Abilities: Strategically approaches assignments with thorough understanding of customer needs, product attributes, revenue generation, profit and loss analysis. Skilled at making presentations to all levels. Seen as a relationship builder and resource integrator. Demonstrated team selling skills. Strong territory management and organizational skills.

Relationship Skills: Demonstrated strong interpersonal skills. Relates well to all kinds of people, up, down, and sideways, inside and outside the organization. Builds constructive and effective relationships. Uses diplomacy and tact; truly values people; can diffuse even high-tension situations comfortably.

Business Acumen/Skills: Can well balance strategic and business actions. Good understanding of current and possible future market trends, sales initiatives, and information affecting the business and organization. Knows the competition; is aware of how strategies and tactics work in the marketplace. Has led and/or participated on project teams with sound understanding of project management. Has good judgment about which creative ideas and suggestions will work; has a sense about managing the creative process. Sees ahead clearly; can anticipate future consequences and trends accurately; has broad knowledge and perspective.

EDUCATION AND EXPERIENCE:

Bachelor's degree with course work in the biological sciences, including Medical Technology. Prior clinical microbiology lab experience preferred. Business experiences in a science related field a plus.

Minimum of 3 years prior selling experience, preferably in capital equipment. 3 - 5 years documented sales success (top 20%). A combination of clinical market sales, financial and technical selling experience required. Computer savvy with multiple software applications.

Job
Sales Representative / Account Management

Primary Location
CA-Quebec

Other Locations
CA-Quebec-Montreal

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/QUEBEC-CDN-INSTRUMENT-SALES-SPECIALIST,-BDB-Job-CA/702153/7021537021532010-04-10BDfull-timeUSDstarting0BSMontreal, QUEBEC, CA
Description

General Function

Reporting to the Business Director, this role will be responsible for the management and development of a high performance team consisting of marketing and clinical associates. This individual will be accountable for the overall development and execution of the Medical Surgical and Ophthalmic business strategy working in close alignment with the Sales Team and Strategic Account Management group to ensure continued growth and profitability.

Key Responsibilities

* Coach and mentor 3 product managers, 1 Technical Services representative and 3 Clinical Specialists, 1 Clinical Education Specialist; ensuring development plans, IIG's and HR planning are in place and reviewed quarterly at a minimum.
* Accountable for the overall Medical Surgical and Ophthalmic product portfolio, including P&L responsibility, forecasting, and strategy development as it relates to both short term and long term financial planning.
* Ensure effective communication amongst sales, marketing and clinical teams within BD Medical as well as across other business units, with the end goal of enhancing business strategies and accelerating sales growth.
* Leverage internal clinical expertise throughout the sales process and ensure it is a component of marketing strategies.
* By providing strategic, tactical and marketing leadership, assist product managers with the development and execution of their marketing plans.
* Responsible for ensuring clinical and marketing cost centres to achieve budgeted goals and ultimately, net sales and OIBT targets.
* Maintain key relationships with the global BD Medical Surgical organization both for themselves and their marketing and clinical team.
* Demonstrate leadership and participate in the S&OP process, contributing to its continuous improvement and achievement of business excellence with respect to KPI's.
* Management of overall pricing strategy and GP targets

Qualifications

Position Requirements

Demonstrated strategic marketing, people development skills, initiative and business acumen

Minimum five years marketing experience; previous market manager experience an asset

University Degree in business and/or science.

Nursing or clinical equivalent background preferred

Strong analytical and negotiating skills with the capability of communicating with all management levels.

Have strong project management skills with the ability to assess and judge appropriate project priorities.

Working knowledge of clinical workflow in acute-care settings

Knowledge of PIR process, S&OP process

Sales experience an asset

Job
Strategic Marketing / Planning

Primary Location
CA-Ontario-Mississauga

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/ONTARIO-Marketing-and-Clinical-Manager-Job-CA-91710/702154/7021547021542010-04-10BDfull-timeUSDstarting0BSMississauga, ONTARIO, CA
BD Biosciences, a segment of BD, is one of the world's leading businesses focused on bringing innovative research and clinical tools to life scientists and clinicians. Its product lines include: flow cytometers; cell imaging systems; monoclonal antibodies; research reagents; diagnostics assays; and tools to help grow tissue and cells.

BD is an EEO/AA employer

About us

Description

JOB SUMMARY

Responsible for providing field-based advanced applications specialist support for BD Cell Analysis products, concentrating efforts in the BioImaging segment. Serve as a technical resource for BD Cell Analysis BioImaging sales and other field associates and BD Cell Analysis BioImaging customers. Uses technical expertise in cell analysis applications to support BD Cell Analysis reagent and instrument customers, in alignment with BD business initiatives. Serve as a technical resource for in-house departments. Works independently without direct supervision. This is a field based position and will ideally be located in Northeast region of the United States.

DUTIES AND RESPONSIBILITIES

Provide on-site / electronic technical consultation to BD customers on BD Cell Analysis products, with emphasis for BioImaging support. Record customer contact information and interests; provide that information to in-house resources as necessary.

Provide on-site / electronic technical consultation with BD Sales Associates on BD Cell Analysis BioImaging instruments and reagents. Maintains high level of expertise in instruments, reagents and software (and applications) and develops expertise on new products.

Assist with BD Sales with instrument and applications demonstrations in workshop form, or as a bona fide product demonstration.

Assist with assay development, which may include assay validation. Provide feedback into Marketing to make adjustments to applications where necessary and required. Perform assay and instrument problem troubleshooting consultation to customers, on-site or via phone / web-based services. Provide information the Field Service on instrument status. Report on problems to appropriate in-house resource. Follow-up to track resolution of issues.

Identify significant scientific trends or new issues of strategic importance and communicates them to BD field or in-house resources as appropriate. Participate in product incident report/customer complaint reporting systems.

Provide on-site support for sales/marketing events, including technical support for trade shows, Marketing sponsored seminar series, and users' meetings.

Perform hands-on customer workshops for instruments and assay systems. Assist customers with assay development and implementation.

Develop and deliver technical presentations. Consult with Marketing and Sales to develop product promotional materials in alignment with BD business initiatives.

Keep abreast of the basic requirements for compliance in own area of work and complies with those requirements. Participate as required in training on regulatory issues affecting own area of work. Bring regulatory compliance questions/issues to the attention of management.

Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participate in Environmental Health and Safety programs. Address corrective actions whenever a hazard is identified. Notify supervisor of all observed hazardous conditions or unsafe work practices.

Travel for on-site support approximately 70%. Maintain reasonable travel budget in alignment with BD practices.

Perform other related duties and assignments as required.

Qualifications

Qualifications:


A minimum of a Bachelor's degree

A minimum of 5 years Image acquisition / analysis experience

Ability to travel a minimum of 70% of the time

A valid driver's license.

Assets:


Experience with current cell biology academic discipline highly desired.

Individuals with a degree in a life science field preferred.

Previous experience with BD BioImaging instrumentation, specifically BD Pathways BioImagers, is highly desired.

Previous experience with flow cytometry / cell sorting desired.

Previous experience providing onsite technical customer support.

Previous technical demonstration experience in support of Sales.

Thorough knowledge of Pharmingen and BDIS products.

Effective analytical, troubleshooting, and problem solving skills.

Effective interpersonal, written and oral communication skills.

Effective organization and planning skills.

Job
Technical / Field Service

Primary Location
United States

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/UNITED-STATES-Technical-Applications-Specialist-Job/702158/7021587021582010-04-10BDfull-timeUSDstarting0BSUnited States
Description

JOB SUMMARY

Maintain buildings, laboratories, offices, lobby areas, kitchens and restrooms in a clean and sanitary condition. Duties include, but are not limited to: dust and wipe all flat surfaces, shelves, counters, clean kitchen/sink areas, restock/refill paper supplies, empty trash, sweep & dust mop floors, vacuum carpeted areas, clean and sanitize restrooms, etc. He/she works safely and follows good housekeeping procedures.

DUTIES AND RESPONSIBILITIES

Safely performs the following responsibilities according to established Standard Operating Procedures and Good Housekeeping Principles:

1. Maintains buildings, laboratories, offices, lobby areas, kitchens, and restrooms in a clean and sanitary condition according to principle responsibilities schedule.

2. Dusts and wipes all uncluttered flat surfaces, shelves, air vents and counters.

3. Cleans all sinks, all kitchen areas.

4. Restocks all kitchen areas with paper, plastic, and styrofoam products, coffee, tea and other related items.

5. Refills all soap, paper towel, feminine hygiene, napkin and tissue dispensers.

6. Empties trash from offices, labs, and patios.

7. Sweeps floors and vacuums carpets.

8. Damp mops floors, removes spots/spills/stains.

9. Strips and waxes floors as required. Buffs floors as required.

10. Spot cleans walls, mirrors, doors, glass, damp clean tops of doors, ledges, sills, and furniture.

11. Cleans and sanitizes toilets and urinals.

12. Sweeps and hoses down exterior walks, stairs and patios.

13. Safely handles and disposes of paper trash, lab glass and lab waste (including biohazard trash) products daily. Places all trash into appropriate containers to avoid exposure or injury to self or others.

14. Moves furniture as needed to clean floors.

15. Reports location of dangerous or unsightly conditions, corrects if possible.

16. Works safely and carefully especially in laboratory areas. Uses all machines, tools and chemicals associated with housekeeping safely and in the manner intended by the manufacturer.

17. Works non-standard hours, eight hours per day which may include weekends and holidays as scheduled.

18. Works overtime hours when scheduled to complete special projects or needs.

19. Demonstrates ability to plan, organize, and carry out details of own work schedule efficiently and completely without routine overtime work hours.

20. Openly participates in job related discussions with Custodian Supervisor for the betterment of the company and self.

21. Obtains cleaning supplies from main storage areas as required to maintain sanitary building conditions. Notifies supervisor when inventory stock levels are low and need reordering.

22. Utilizes appropriate personal protective equipment.

23. Operates various Company vehicles in a safe and responsible manner and maintains appropriate vehicle usage records/documentation.

Qualifications

MINIMUM QUALIFICATIONS

KNOWLEDGE AND SKILLS

· Strong working knowledge of good housekeeping principles is a must.

· Must have a demonstrated experience working with cleaning chemicals and machines.

· Must have good oral and written communication skills.

· Must be attentive to details; neatness and accuracy is important.

· Must be able to work with minimum supervision on a flexible schedule.

· Basic computer proficiency is necessary.

· A valid, unrestricted California driver's license and a clean driving record are required.

PHYSICAL REQUIREMENTS

Must be able to perform continuous lifting of 10 to 15 pounds and rare/occasional lifting of 25 to 50 pounds without assistance.

Continual walking, reaching, pushing, stooping, grasping, lifting throughout the workday.

EDUCATION AND EXPERIENCE

A high school diploma is required
Requires a minimum of 1 year custodial experience

Job
Other

Primary Location
US-California-San Diego

Shift
Second Shift / Afternoon Start

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-DIEGO-Custodian-Job-CA-92101/704029/7040297040292010-04-10BDfull-timeUSDstarting0BSSan Diego, CA, US
Description

JOB SUMMARY

Maintain buildings, laboratories, offices, lobby areas, kitchens and restrooms in a clean and sanitary condition. Duties include, but are not limited to: dust and wipe all flat surfaces, shelves, counters, clean kitchen/sink areas, restock/refill paper supplies, empty trash, sweep & dust mop floors, vacuum carpeted areas, clean and sanitize restrooms, etc. He/she works safely and follows good housekeeping procedures.

DUTIES AND RESPONSIBILITIES

Safely performs the following responsibilities according to established Standard Operating Procedures and Good Housekeeping Principles:

1. Maintains buildings, laboratories, offices, lobby areas, kitchens, and restrooms in a clean and sanitary condition according to principle responsibilities schedule.

2. Dusts and wipes all uncluttered flat surfaces, shelves, air vents and counters.

3. Cleans all sinks, all kitchen areas.

4. Restocks all kitchen areas with paper, plastic, and styrofoam products, coffee, tea and other related items.

5. Refills all soap, paper towel, feminine hygiene, napkin and tissue dispensers.

6. Empties trash from offices, labs, and patios.

7. Sweeps floors and vacuums carpets.

8. Damp mops floors, removes spots/spills/stains.

9. Strips and waxes floors as required. Buffs floors as required.

10. Spot cleans walls, mirrors, doors, glass, damp clean tops of doors, ledges, sills, and furniture.

11. Cleans and sanitizes toilets and urinals.

12. Sweeps and hoses down exterior walks, stairs and patios.

13. Safely handles and disposes of paper trash, lab glass and lab waste (including biohazard trash) products daily. Places all trash into appropriate containers to avoid exposure or injury to self or others.

14. Moves furniture as needed to clean floors.

15. Reports location of dangerous or unsightly conditions, corrects if possible.

16. Works safely and carefully especially in laboratory areas. Uses all machines, tools and chemicals associated with housekeeping safely and in the manner intended by the manufacturer.

17. Works non-standard hours, eight hours per day which may include weekends and holidays as scheduled.

18. Works overtime hours when scheduled to complete special projects or needs.

19. Demonstrates ability to plan, organize, and carry out details of own work schedule efficiently and completely without routine overtime work hours.

20. Openly participates in job related discussions with Custodian Supervisor for the betterment of the company and self.

21. Obtains cleaning supplies from main storage areas as required to maintain sanitary building conditions. Notifies supervisor when inventory stock levels are low and need reordering.

22. Utilizes appropriate personal protective equipment.

23. Operates various Company vehicles in a safe and responsible manner and maintains appropriate vehicle usage records/documentation.

Qualifications

MINIMUM QUALIFICATIONS

KNOWLEDGE AND SKILLS

· Strong working knowledge of good housekeeping principles is a must.

· Must have a demonstrated experience working with cleaning chemicals and machines.

· Must have good oral and written communication skills.

· Must be attentive to details; neatness and accuracy are important.

· Must be able to work with minimum supervision on a flexible schedule.

· Basic computer proficiency is necessary.

· A valid, unrestricted California driver's license and a clean driving record are required.

PHYSICAL REQUIREMENTS

Must be able to perform continuous lifting of 10 to 15 pounds and rare/occasional lifting of 25 to 50 pounds without assistance.

Continual walking, reaching, pushing, stooping, grasping, lifting throughout the workday.

EDUCATION AND EXPERIENCE

A high school diploma is required
Requires a minimum of 1 year custodial experience

Job
Other

Primary Location
US-California-San Diego

Shift
Second Shift / Afternoon Start

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-DIEGO-Custodian-Job-CA-92101/704030/7040307040302010-04-10BDfull-timeUSDstarting0BSSan Diego, CA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD Diagnostics - TriPath develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Physician Sales Representative is responsible for calling on OB/GYN physicians within an assigned territory. He/She must provide the physician with complete information pertaining to the assigned BD product lines in a manner that will ensure the appropriate use of these products and achieve the required business growth. This includes the capability of transporting and effectively demonstrating the BD Affirm™ instrument to medical professionals and understand the CLIA licensing process. This will include the ability to effectively present an economic model tailored for the customer. This individual is responsible for sales, marketing feedback, and customer satisfaction and must be able to work effectively with BD distributors to close new accounts.

This position will be located in the Richmond, VA area.

Principal Accountabilities:

1. Invest the time and the effort to achieve the established goals for the territory such as sales quotas, market share, product evaluations, etc.
2. As directed by the RSM or RBM, work with the Laboratory Account Executive as a member of the local account team to implement business strategies
3. Represent BD Diagnostics - TriPath at local, regional, and national meetings and conventions as required.
4. Plan and organize daily sales call activities to optimize the use of time and maximize the achievement of sales and market share objectives
5. Record all sales call activates on a daily basis and entering that data in the SFA system for tracking
6. Maintain timely and relevant communication with the RSM or RBM and other members of the local account team
7. Effectively communicate competitive information and market information on a timely basis
8. Manage territory expenses within guidelines and ensure that all expense reports are accurate and submitted by the required deadline

Job Dimensions

· Number of Direct Reports: 0

· Travel Requirement: Limited overnight travel required in some territories

· Geographical Responsibility: Varies with assigned territory

· Sales Responsibility: Varies - Up to $3,000,000

Qualifications

Education and Experience Required:

· A Bachelor's degree (BA or BS) from a four year college or university

· Minimum of 3 years medical sales experience

· Ability to read, analyze, and interpret documents such package inserts, professional journals, technical procedures, and government regulations

· Computer proficiency is required, including skills with the use of Microsoft Word, Excel and PowerPoint

· Comprehensive knowledge of current U.S. healthcare trends that can be integrated into territory sales strategies

· Well developed organizational and time management skills

Education and Experience Preferred:

· Sales experience in the OB/GYN market

Job
Field Sales

Primary Location
US-Virginia

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/US-Physician-Sales-Representative-Richmond,-VA-Job-VIRG/705319/7053197053192010-04-10BDfull-timeUSDstarting0BSUS-Virginia
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

About us

Description

High Impact position responsible for developing & executing strategies for sustainable medical device packaging, supporting BD's environmental sustainability initiative.

The candidate will be a dedicated Technical Lead for identifying, managing & delivering green packaging for new and existing medical devices across multiple product platforms. Specific responsibilities include,

* Bring expertise in designing for green and life cycle analysis in identifying & evaluating materials, designs, and configuration of primary, secondary, and other packaging levels, as applicable, optimizing carbon footprint, customer benefit and the supply chain requirements
* Identify, evaluate & recommend new packaging materials for cost effectiveness, recyclability & re-usability
* Development and Validation (per design control requirements) of packaging components, designs and processes/technologies for various sterilization modes preserving the safety and efficacy over the shelf life
* Evaluates new packaging concepts and technologies using engineering first principles
* Create prototypes, drawings, specifications, test instructions for customer approval, external testing and tooling requirements.
* Work directly with suppliers to qualify new materials / designs
* Visit / interview external customers to gather Voice of customer related to packaging
* Proactively develops and maintains technical knowledge in specialized area(s), remaining up-to-date on current trends and best practices. Actively teach and promote learning.
* Provide Project Leadership to cross-functional teams comprising QA, purchasing, product R&D, MA, RA, marketing, manufacturing engineering, sterilization sites.
* Independently plan, implement, delegate, monitor and deliver designated tasks and deliverables.
* Effectively lead and direct the work of other engineers and laboratory technicians to achieve objectives.
* Ensure compliance with BD quality policies, procedures and practices as well as with all local, state, federal and BD safety regulations, policies and procedures.

Qualifications

*
Minimum: MS degree in Materials Science, Industrial Design or other technical discipline (Polymers, Design, Mechanical, Packaging) with at least 4 - 6 years direct, relevant experience.

*
Experience in the medical device or pharmaceutical industry is preferred.

*
Ph.D. in above disciplines with 2 years relevant experience is preferred

*
Lean / Six Sigma preferred

*
Design packages for green consideration

*
Experience developing packaging green strategy

*
Life cycle analysis and strategic tradeoff between materials/ design

*
Experience in at least one environmental sub-field, such as carbon accounting, life cycle assessment, sustainable materials, or waste management

*
Experience with rigid and flexible forming materials and technologies (corrugate, paper board materials, F/F/S, Flow wrap)

*
VOC analysis

*
Experience with Package processing equipment & process development package loading

*
On line labeling & printing experience

*
Familiarity with blow molding, injection molding, and film extrusion

*
Leading Lean/Six Sigma projects preferred

* Fundamental package design principles & techniques
*

Packaging design software (e.g. TOPS, CAPE, ArtiosCAD)

*

Excellent cross-functional influencing skills

*

Understanding of disciplined product development processes

*

Strong Organization skills

*

Sound technical judgment

*

Working knowledge of ISO, FDA and international regulatory and quality requirements applicable to Medical Device Packaging

*

Knowledge of environmental science principles and ecological impacts

*

Design and statistical analysis of experiments

*

Project planning

*

Value stream analysis, preferred

Job
Materials Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Principal-Engineer-Job-NJ-07417/705320/7053207053202010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

JOB SUMMARY:

Under the direct supervision of the Plant Controller or Cost Accounting Supervisor, the Sr. Cost Accountant has complete financial responsibility for approximately one - two plant(s) and/or financial responsibility for a group of operational cost centers. Duties cover all facets of cost accounting, and include but are not limited to, budgeting, forecasting, standard cost development, reporting and analyzing manufacturing variances and maintaining fixed assets for the assigned plant(s). The Senior Cost Accountant also actively participates on the Executive Steering Committee, which includes presenting monthly operating results and responding to inquiries.

DUTIES AND Responsibilities:


* Conduct monthly closing activities, including preparation of journal entries, reconciliation of general ledger accounts. Ensure transactions are prepared in accordance with GAAP. Also prepare required monthly/quarterly reports.
* Provide financial leadership to the assigned plant(s) and operational departments related to financial results, budgeting, forecasting and ESC (Executive Steering Committee) membership.
* Perform analyses of manufacturing variances and provide operations with assistance in determining the reasons for these variances. Develop reports and analyses to interpret trends in variation from standard and recommend/discuss corrective actions with the plant leadership.
* Prepare the annual budget for the assigned plant(s) including presentation of the plant's/department's standard costs and cost changes, labor and overhead expenses and associated plant variances to Operations and Financial management.
* Compile information from plant in order to prepare the quarterly forecast.
* Complies with Sarbanes-Oxley internal controls and participates in testing.
* Perform reconciliations and analysis of general ledger accounts as required.
* Maintain record of fixed assets for the plant in accordance with Corporate policy.
* Work with various groups in the plant to obtain information to measure and track the impact of cost reduction initiatives (Six Sigma, Plant Teams, Continuous Improvement).
* Participate and represent Cost Accounting on plant leadership teams and other cross-functional project teams such as SAP teams, company-wide manufacturing teams and GPDS (Global Product Development Systems) finance representation.
* Provide leadership and mentorship to other cost accountants as needed.

Qualifications

MINIMUM Qualifications:


KNOWLEDGE AND SKILLS:

· Advanced skills in Excel as demonstrated by previous experience creating and manipulating complex spreadsheets.

· Proficient in Microsoft Word and PowerPoint.

· Prior SAP costing experience related to standard cost build-ups and workorder variance analysis is preferred.

· Ability to summarize complex issues and present to all levels of management.

· Ability to effectively communicate to, and work with, associates at all levels, up to and including, management / plant management and those in remote locations.

· Ability to function in a team environment.

EDUCATION AND EXPERIENCE:

· B.S. in Accounting / Finance

· Minimum 3-5 years of cost accounting experience in a manufacturing environment.

Job
Cost Accounting

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Senior-Cost-Accountant-Job-MD-21201/705571/7055717055712010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
Description

The Technical/Clinical Services Specialist is responsible for providing clinical leadership with respect to BD MedSurg products, their intended uses and clinical/technical applications to a network of end-user customers, distributors and sales representatives. This role is the central link between the MedSurg sales and marketing team and the Quality and Regulatory Department both in Canada and at a global level.

Some key responsiblities include:

·Provide telephone technical consultation to end-user customers, distributors, field sales and internal personnel regarding product specifications, "best practice" techniques and available substitutions pertaining to BD MedSurg products.

·Act as liaison between the BD MedSurg sales association, the end-user customer, the distributor network and BD MedSurg business to resolve technical/clinical issues and customer problems or issues.

·Document all product incident reports (PIR's) according to BD MedSurg Quality Procedures Guidelines.

·Create, deliver and maintain a PIR education program and the accompanying tools for the sales organization.

·Monitor PIR's for trends and alert Quality & Regulatory for possible recalls; participate in recall process.

·Create quarterly reports on complaint trends and present to MedSurg management team.

Qualifications

Registered Nurse with a bachelor's degree in nursing

Minimum 5 years experience in Acute Care nursing

Experience in an industry related/customer-facing role an asset

Extensive interpersonal and problem solving skills

Able to work independently and in a team environment

Presentation skills an asset

Working knowledge of Microsoft Office

Being fully bilingual would be an asset but not a requirement

Ability to travel a minimum 15% - 20% of time.

Job
Other

Primary Location
CA-Ontario-Mississauga

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/ONTARIO-CDN-TECHNICAL-CLINICAL-SERVICES-SPECIALIST-Job-CA-91710/705574/7055747055742010-04-10BDfull-timeUSDstarting0BSMississauga, ONTARIO, CA
Description

Responsible for the sales and promotion of Ophthalmic Disposable Instruments in the New England Territory. Target call points will be hospitals and ambulatory surgery centers. Territory coverage will be MA, ME, RI, CT, NH, VT.

Scope of Responsibility:

· Strategic Impact/Accountability Responsible for maintaining and growing annual sales volume in assigned territory. Reports to the Regional Business Manager.

· Required Skills and Knowledge B.S./B.A. Degree in Business and/or related medical field.

· Technical Area of Expertise 3-5 years selling experience

preferably in the health care market. Ophthalmic experience a plus.

· Degree of Accountability (discretion/supervision) Works fairly independently in cooperation with the sales force. Information must be verified to ensure appropriate levels of service to the customers - both internal and external.

.

Qualifications

MINIMUM Qualifications:
3 to 5 years sales experience preferably in the medical industry.

KNOWLEDGE AND SKILLS:

Sales Skills: Exemplifies early adopter behaviors - Absorbs and applies technical information; skilled sales professional. Capably grows technical knowledge base. Knowledge of selling process.

Sales Abilities: Strategically approaches assignments with thorough understanding of customer needs, product attributes, revenue generation, profit and loss analysis. Skilled at making presentations at all levels. Demonstrated team selling skills. Strong territory management and organizational skills. Demonstrated analysis of GP contract models, budgets, expenses.

Relationship Skills: Demonstrated strong interpersonal skills. Relates well to all kinds of people, up, down, and sideways, inside and outside the organization. Builds constructive and effective relationships. Excellent communication skills. Demonstrated team player.

Business Acumen/Skills: Can well balance strategic and business actions. Good understanding of current and possible future market trends, sales initiatives, and information affecting the business and organization. Knows the competition; is aware of how strategies and tactics work in the marketplace. Sees clearly ahead and can anticipate future consequences and trends accurately

EDUCATION AND EXPERIENCE:

Minimum BS degree . Business experiences in a science related field a plus.

Job
Sales Representative / Account Management

Primary Location
US-Massachusetts

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/US-Ophthalmic-Sales-Consultant-Job-MASS/705579/7055797055792010-04-10BDfull-timeUSDstarting0BSUS-Massachusetts
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Job Summary

The Financial Analyst reports to the Manager, Financial Reporting, BD Diagnostics, Infectious Disease Diagnostics, and is responsible for a variety of financial analysis and reporting for Infectious Disease Diagnostics. Provides management with financial direction and analysis of the business actuals, projections and budget submissions. Gives direct support to finance associates on systems and processes. Takes a leading role in the area of internal and Sarbanes Oxley controls for the business. Provides other ad-hoc analyses as required. Finance Core Team Member to multiple cross-functional project teams including supporting complex new product development initiatives.

1. SAP "Super User" to provide both training and system / process support to the business community in general.

2. As Finance Core Team Member for multiple cross-functional project and new product development teams, is an integral part of providing financial support as well as overall business guidance:

* Completes financial model, which includes market analysis, incremental sales analysis, cost estimates, incremental operating expenses. Completes tax haven analysis if applicable. Performs risk analysis and sensitivity analysis for project financials.
* Updates the financial section of the business plans and attends the Commercial Excellence Reviews, Portfolio Decision Team and Project meetings as required.
* Responsible for coordination and writing of Capital Requests and/or assistance in Supply Agreement negotiations.
* Assists Project Team Leaders with expense budgets and projections.

3. Participates as the administrative coordinator for the Sarbanes Oxley control responsibilities - under the manager's direction. Also serves as a reviewer for Sarbanes Oxley requirements as assigned. .

4. Work on monthly closings, and analytical reviews of selected balance sheet accounts.

5. Analyze, evaluate, and provide management with recommendations pertaining to the adequacy of all non-sales related accruals.

6. Responsible for evaluating and updating the monthly financial package distributed to management.

7. Responsible for the preparation, analysis and review of various schedules for the year end tax package.

8. Responsible for the coordination and preparation of various quarter-end and year-end reporting schedules for corporate reporting purposes.

9. Provide audit support and additional support to Finance functional projects or Microbiology business initiatives as required.

10. Travel: 10 -15 % of time will be spent working at BD locations outside of Baltimore.

Qualifications

Required Knowledge and Skills:

Education and Experience

* B.S. Degree - Major in Accounting, Finance, Business or related area.
* MBA or graduate degree in accounting desirable.
* Four to six years experience in a finance environment including exposure to general accounting, financial analysis, corporate reporting and manufacturing operations with two to four years of general accounting experience required.
* Microsoft Excel, Word, and PowerPoint, SAP, Business Warehouse
* Excellent understanding of financial evaluation techniques.
* Excellent oral and written interpersonal skills are required in order to interact independently with all levels of Business and Corporate management.
* CPA preferred
* Strong knowledge of Generally Accepted Accounting principles (GAAP).
*
Demonstrated understanding of Sarbanes-Oxley controls and testing requirements.

*
Financial modeling for business projects, new products and/or capital expenditures.

Job
Financial Analysis

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Financial-Analyst-Job-MD-21201/706285/7062857062852010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The Quality Assurance Specialist as a member of the Quality Release group is responsible for performing detailed inspections of packaging components (primary and secondary) consisting of visual, mechanical and testing functions and is responsible for all associated paperwork and documentation . This position will also perform sampling of incoming raw materials for QC testing analysis. The Wilson quality system is compliant to 21CFR 210 & 211 and Becton Dickinson Corporate policies. This position will take direction and report to the Quality Release Leader.

Main Responsibilities:


- Member of the Quality Release group responsible for inspection of incoming components, finished product and batch documentation in compliance with 21CFR 210&211, Becton Dickinson Corporate policies, and all other applicable quality / regulatory requirements

- Performs detailed inspections of primary and secondary packaging materials and components using visual, mechanical, and instrumentation methodology
- Perform detailed inspection of finished product samples using visual, mechanical, and instrumentation methodology
- Perform sampling of incoming raw materials per inspection plan for QC testing

- Generate all cGMP documentation associated with work activities
- Enter data/results in SAP and/or SQL LIMS

- Maintain work area and instrumentation in a clean, sanitary, orderly, operational and safe condition
- Perform required standardization on measuring equipment
- Assist in maintaining standard operating procedures
- Performs other related Quality duties as assigned

Qualifications

Required Skills and Knowledge - Bachelors degree in a scientific discipline and 3+ years of relevant Quality Assurance or an associates degree with 10+ years experience in a pharmaceutical manufacturing company. Experience with visual inspection techniques, statistical sampling (ANSI Z1.4 Sampling Plan), ability to recognize defects in materials inspected, ability to work in a fast paced environment, ability to handle a high volume of work and rapidly adapt to changing environment. Prefer an associate trained in six sigma methodology.

Technical Area of Expertise - Good verbal and written communication, organization, prioritization, displays sound judgment, interpersonal and computer competency to perform job. Experience performing investigations and displays good problem-solving skills

Job
Quality Auditing

Primary Location
US-North Carolina-Wilson

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/WILSON-Quality-Assurance-Specialist-Job-NC-27893/706293/7062937062932010-04-10BDfull-timeUSDstarting0BSWilson, NC, US
Description

Reporting to the Engineering Manager, Molding, Manufacturing Process Technology. Responsible for the project management of injection molding tool development in support of new medical disposable product activities. Carries out mold tool development from the prototype stage to full commercial scale tooling and does the process development required to support commercialization.

Responsibilities:


* Interface as part of a cross functional team providing technology input to guide product development on design-for-manufacturability for plastic components.
* Provide project management leadership for the injection molding tooling required to support a new product.
* Direct activities of tool vendors in sourcing injection mold tooling, conducting design reviews and ensuring on time mold acceptance.
* Direct activities of both cross functional team members and plant personnel in the set up and validation of injection molds at the manufacturing site.
* Evaluate and apply the latest technologies for a competitive advantage over the competition.
* Responsible for maintaining project budgets on both expense and capital spending.

Qualifications

Education:

BS Mechanical or Plastics Engineering required; tool and die maker training a plus.

Experience:

Minimum of eight years experience in injection mold tool technology.

Knowledge of high cavitation, tight tolerance, hot runner injection molds.

Knowledge of plastic part design.

Intimate knowledge of thermoplastic technologies, molding materials and high speed assembly technology.

Knowledge of Scientific Molding priciples in plastic processing.

Knowlwdge of Mold Validation Procedures following IQ, OQ and PQ format and DOE's

Job
Project Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Project-Engineer-Molding-Job-NJ-07417/707822/7078227078222010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

Core Team Leader leads the cross-functional Core Team and Extended Team in executing all aspects of product development project including effective requirements management and the subsequent transition into commercialization including achievement of defined strategic and financial objectives. Core Team Leader is responsible for leading all aspects of product development from the start of the Definition Phase through successful completion of the Launch Phase (i.e. commercialization and transition of product into normal business operations or Life Cycle Management processes). A Core Team Leader is ultimately responsible for the execution quality and results of his or her project and the success of the resulting product in the market. Core Team Leaders may have different levels of proficiency in various aspects of the role. Senior Core Team Leader should be capable of managing varying degrees of program and project size, cost, complexity or risk.

Responsibilities

The Core Team Leader is responsible and accountable to lead and direct cross-functional activities and outcomes including:

* Defining, refining, and understanding customer requirements.
* Architecting or refining the high-level product concept to fulfill the customer requirements.
* Leading the creation of the cross-functional project plan, including budget and resource planning, to fulfill the product concept.
* Resolves personal/team conflicts and project/functional conflicts.
* Aligning and managing all cross-functional activities to deliver the product on time and on budget per contract while meeting all agreed upon technical, operational, business and customer requirements.
* Providing work definition and direction to the assigned cross-functional Core Team Members.
* Providing coaching and mentoring to Core Team members and providing significant feedback to functional leaders regarding training needs of, and resources required by, the core team.
* Providing meaningful and significant input to the performance of core team members that is fully considered in their year-end performance reviews and compensation recommendations.
* Successful commercial, design, and business project reviews; makes PDT aware of, and proposes solutions to, unanticipated or potential issues/concerns as soon as they are known.
* Successful product design.
* Superior product quality in the field.
* Product acceptability by intended customers; spends time with customers/end-users and constantly invests in understanding customer environment.
* Successful product commercialization.
* Completion of accurate and timely reporting, e.g. project portfolio server (G3), resource allocation, dashboard updates.
* Contributes to the continuous improvement in organization's ability to execute programs and projects from initiation through launch.
* Coaching and mentoring new Core Team Leaders.

Experience

* Demonstrated proficiency or mastery in defined competencies and a minimum of 10 years experience leading teams.
* Prior Core Team Leadership on complex line extensions and new products.

Qualifications

Requirements include BA/BS degree. MBA preferred. PMI certification a plus. In addition, demonstrated strength in business acumen along with the breadth of technical, organization, and leadership capabilities, including strengths or potential in most of the following skills/competency areas:

* Innovative and Conceptual Thinking
* Cross-Functional Leadership
* Product Architecture
* Cross Functional Leadership
* Managerial Skills
* Project Leadership/Mgmt
* Personal Effectiveness

Core Team Leaders exhibit behaviors that enable them to fulfill their accountabilities. Below is a sample of key behaviors .

* Spends time with customers and end users to understand customer environment and constraints, customer processes and workflow, and unmet needs and how to fulfill them.
* Effectively challenges and directs all cross-functional work products based on cross-functional expertise, aptitude, experience, and skills.
* Challenges business leadership with facts and alternate recommendations, willing and able to recommend that the PDT stop the project if necessary, and demonstrated loyalty to business success versus project.
* Effectively leads the Core Team to make tradeoffs between schedule, scope and resources within the boundaries of the project contract.
* Seeks out guidance and training from functional leaders in order to better lead Core Team activities and members.
* Willing to challenge non value-added policies and procedures.
* Takes decisive action when Core Team Members are not performing or delivering, communicates missed expectations directly including contact with functional managers.
* Maintains 2-way communication with Core Team Members, Functional Managers, and PDT Members in the context of roles and accountabilities (e.g. Core Team Members are the primary communication method to Functional Managers).
* Focuses Core Team meetings on looking ahead at program issues and risks, identifying the need for and initiating technical and business reviews, anticipating future risks and initiating risk mitigation.
* Drives the team to consensus but is able to "cap" the discussion and make decisions.
* Acknowledges mistakes and communicates lessons learned.
* Incorporates appropriate tools and methodologies into the development effort that make the team more effective.
* Maintains awareness of current and future possible policies, practices, trends and information that could impact the program or the overall business.

Knowledge of specific procedures/practices

* GPDS Processes and Procedures
* Technology Development Process
* Product Development Performance Metrics
* Preliminary and Integrated Business Plans
* DFSS/DFMA
* Post Launch Reviews
* Voice of Customer Methodologies
* Team Formation and Dynamics
* Project Management

Job
Project Management

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKES-Core-Team-Leader-Job-NJ-07417/707824/7078247078242010-04-10BDfull-timeUSDstarting0BSFranklin Lakes, NJ, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

About us

Description

The System Support Specialist (SSS) functions as the senior technical expert within the Service organization. The individual has seven distinct Responsibilities:


1. Prepare the Service organization worldwide to support new products
2. Advise Service Management on departmental strategies to assure quality support and service worldwide
3. Develop and update departmental procedures
4. Develop, support, and train System Support personnel
5. Actively participate as a project Core Team member as part of the Global Product Development Process
6. Effectively manage multiple new product launches
7. Establish new product failure reporting during the initial stages of the product life cycle

Individuals must be consistently professional in customer and cross-functional interactions with acute attention to customer needs and expectations. Candidates will have experience in applying an interdisciplinary, collaborative approach to plan, design, develop, and verify system solutions. Candidates will evaluate customer/operational needs to define and coordinate system performance requirements, integrate technical parameters, and assure compatibility of all physical, functional, and program interfaces. Individuals will provide connectivity support and training to internal and external customers. Items under the connectivity umbrella include but are not limited to: LIS interfaces, networking, middleware, computer software and integration projects, and device relationship management

Motivation, self-confidence, persuasiveness, perseverance, a professional and outgoing personality, a willingness to contribute at all levels, and an excellent understanding of customer service are required. Individuals will monitor work to ensure quality, and continuously promote Quality First Time. These individuals handle more difficult problem solving challenges by leading the troubleshooting analysis, planning the action response, following up to ensure customer satisfaction

Duties include monitoring project status and reporting Service issues to Program Managers. Individuals are often responsible for managing logistics for clinical and beta sites, R&D trials, and trade shows. Candidates will coordinate service and development efforts with customers, technical support (in house and field based), marketing, R&D, project teams and LIS vendors. They may travel to customer sites, and attend meetings as determined appropriate by Management.

Qualifications

Required Skills:

* Bachelor's Degree in a related technical discipline.
* A minimum of five years previous service experience with networking, LIS interfaces, servers, software, hardware, and computers.
* A minimum of three years Project Management experience is required.
* Knowledge of hospital interfaces, middleware concepts, and applications is essential.
* Previous experience training, presenting or demonstrating complex systems highly desired.
* Excellent written and oral communication skills to resolve complex network and server related issues into actionable concepts for customers to understand.
* Strong interpersonal skills and the ability to effectively communicate at all levels of the organization.
* Possess ability to make independent decisions with far reaching impact.
* Possess ability to work through issues and bring projects to completion; perform complex research, analysis, and troubleshooting; and resolve critical problems over sustained time durations in a logical manner.
* Strong organizational skills, detail orientation, the ability to multi-task, meet deadlines, and prioritize work
* Superb customer facing skills
* Must be able to travel internationally

Job
Technical / Field Service

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-System-Support-Specialist-Job-MD-21201/707825/7078257078252010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The Marketing Communications Manager has responsibility for managing the creative development process for marketing communications programs for multiple product lines. Responsible for giving direction to the creative resources available (agency, Creative Services group, outside vendors) which includes ensuring that budgets, schedules, and performance requirements are met by creative resources. Scope includes development and production of printed literature/advertisements; management of trade shows, symposia and conventions; management of electronic commerce initiatives. Success of this position relies on pro-active involvement with BDB marketing managers worldwide to assure both worldwide brand strategy initiatives, as well as local marketing programs, are supported efficiently and effectively. Works on problems of diverse scope where analysis of situations or data is required. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining results. Normally receives no instruction on routine work, general instructions on new projects.

Responsible for overall product positioning in the market, including messaging and promotional programs by channel. Establishes, implements and maintains "best practices" in marketing communications. This position requires 25% travel (domestic and international).

Qualifications

Typically requires a BS/BA, Biology or related field preferred; MBA desired. Requires a minimum of 5 years of directly related marketing communications experience to include working with vendors on a national level; development and execution of brand strategy initiatives; promotional lit design and production, or equivalent combination of related education and experience.

* Strong project management and planning skills. Results oriented, capable of managing and driving the completion of multiple competing projects
* Must possess excellent written and oral communication skills, including effective presentation skills.
* Ability to thoroughly edit marketing communications pieces for accuracy, grammar, typos, and graphic content.
* Ability to manage production of marketing communication pieces including final artboards, bluelines, and press proofs.
* Thorough knowledge of print production.
* Knowledge of graphic design concepts.
* Demonstrated web development skills and working knowledge of electronic commerce.
* Must have advanced skills in Macintosh, Word and PowerPoint.
* Effective organization, decision making and problem solving skills.
* Effective leadership and interpersonal skills.
* Working knowledge of bioprocessing market & related merchandising/promotional support preferred.

Job
Marketing

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BALTIMORE-Marketing-Communications-Manager-Job-MD-21201/708490/7084907084902010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

Working out of the Bedford, MA office and reporting to the R&D Manager, this position applies intensive and diversified knowledge of polymer surface chemistry to be used for modification of surfaces using synthetic and biological molecules. The position will identify and develop surfaces to be used to modulate phenotype of mammalian cells in vitro.

DUTIES AND RESPONSIBILITIES

* Using independent judgment and interpretation, applies basic scientific principles and personal technical expertise to accomplish product application, design and development objectives.
* Conceptualizes, prioritizes, schedules, and execute project deliverables.
* Individually and as part of a multi-functional team, determines risk associated with particular design directions and judges impact on project.
* May lead or participate on cross functional product development team.
* Determines scope of work for project tasks and establishes schedules.
* Designs and assesses the feasibility and soundness of proposed surface chemistry evaluation tests, products, or equipment and analyzes and reports on resulting data.
* Must effectively present/communicate technical data to others
* May review and prepare patent applications and manuscripts for publication or presentation at technical meetings.
* Responsible for calibration and upkeep of designated instruments and equipment.
* Provides technical training and support for QC, Production, Sales staff, Customers, others.
* Assist in resolving technical issues with customers (travel to visit customers, as necessary).
* Assist in the preparation and review of marketing and sales literature.
* Other projects as required.

Qualifications

* Experience with cell culture, cell / surface interactions and biomolecule / surface interactions.
* Understanding and practical utilization of methods of surface analysis such as FTIR, ESCA, and related surface analytical tools.
* Experience with the immobilization and covalent conjugation of biomolecules (peptides and proteins) and small molecules on surfaces.
* Experience with surface modification and coating techniques, especially the modification and coating of polymeric surfaces.
* Experience with the coating of polymers and hydrogels on surfaces.
* Experience with surface characterization techniques including contact angle measurements, surface functional group chemical assays, and immobilized biomolecules concentration analysis.
* Experience with product development
* Oral and written presentation skills and publication of peer-reviewed papers.
* Strong competence in data analysis is essential.
* Ability to find innovative approaches to unmet needs
* Ph.D. with 10 years experience in Life Sciences, Chemical Engineering, Organic/Synthetic Chemistry or Polymer Science
* Industrial experience required

Job
Life Sciences R & D

Primary Location
US-Massachusetts-Bedford

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/BEDFORD-Surface-Chemist-Job-MA-01730/708967/7089677089672010-04-10BDfull-timeUSDstarting0BSBedford, MA, US
BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public.

BD is an Equal Opportunity/Affirmative Action Employer

About us

Description

The QA / RC Manager is responsible for the management and continuous improvement of site quality systems. This requires oversight of nonconforming materials, including field corrective actions. This manager will guide quality related decisions regarding the development of new products and changes in current products; including oversight of manufacturing processes testing protocols and inspection criteria. This will require insuring the functional excellence of the new product development process and the Validation program. The manager is responsible for finished product quality via final product inspection and release. The manager will support both internal, external, regulatory and customer audits.

The Manager is expected to interact with other BD plants and regions, external customers, suppliers and regulatory agents. Must be familiar with existing national and international governmental regulations (21 CFRs, DOT, USDA, ISO 9000 etc.).

Complies with all local, state, federal and BD safety and quality regulations, policies, practices and procedures. Performs other duties as assigned.

Qualifications

Education: Minimum requirements for this position include a Bachelor of Science degree in a scientific discipline. Computer skills (SAP, MS Word, PowerPoint and Excel; and Filemaker) are essential.

Work Experience: Three to eight years QA/RA experience in an industrial /manufacturing environment is required. This must include at least 3 years validation experience in biologics product development and manufacturing environment. Management or supervisory experience in quality control, quality assurance or regulatory affairs required.

Job
Quality

Primary Location
US-California-San Diego

Shift
First Shift / Day Job

Relocation Available
No]]>http://www.bd-careers.com/job/SAN-DIEGO-Quality-Assurance-Manager-Plant-Job-CA-92101/708968/7089687089682010-04-10BDfull-timeUSDstarting0BSSan Diego, CA, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 28,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

The R&D Senior Scientist will initiate and execute cross-functional projects that support development and production of dehydrated culture media and components for cell culture and microbial fermentation. The successful incumbent will be able to formulate cell culture media, both mammalian and microbial, in liquid and/or powder formats at bench top and pilot scale. This position will also be responsible for formulation and generation of representative pilot samples for internal and external customer evaluations through the use of appropriate scale-down process models. Other duties include process optimization and product enhancement activities, as well as, internal and external communications, such as development of marketing materials and co-authoring or presenting posters or scientific presentations at international conferences.

The Senior Scientist works closely with R&D scientists, Procurement, Quality Engineers, Marketing, as well as, external and internal customers and vendors to define, design and implement solutions for product technical support needs and new product development.

Principal Accountabilities:

· Provide media formulary leadership for functional and cross-functional product activities

· Evaluate customer proprietary media formulations and determine the best manufacturing strategy

· Support Six Sigma tool applications

· Participate in or lead new product development and support activities

· Train associates on newly developed products or assays

· Co-author application notes, posters, presentations, and technical bulletins, for BD product development projects

· Maintain and grow bench skills and expert knowledge of current scientific literature, and state-of-the-art technologies, theories and principles in own area of scientific discipline

· Communicate technical information to both internal and external customers in a team environment

Qualifications

Qualifications:


· Expertise in formulation of powder and liquid cell culture and microbial media

· Track-record of working on or leading teams is required, project management experience is preferred

· Knowledge of media manufacturing processes

· Proficiency with microbiological and/or mammalian cell culture techniques and assays are required

· Research, Industrial or Clinical laboratory experience is required

· Knowledge of Design for Six Sigma or Six Sigma tools is preferred

· Demonstrated excellent interpersonal skills

· Excellent communication skills (written and oral)

· Significant skills in mainstream computer software

Education and Experience Required:
BS degree with 7-10 years, MS degree with 5-8 years or PhD with 2 - 4 years of industry experience or equivalent required. Degree in Chemistry, Cell Biology, Biochemistry, Biotechnology, Microbiology or related science is required. At least two years of Industrial cell culture media formulary experience required.

Job
Life Sciences R & D

Primary Location
US-Maryland-Baltimore

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/BALTIMORE-Senior-Scientist-Formulation-Chemist-Job-MD-21201/709248/7092487092482010-04-10BDfull-timeUSDstarting0BSBaltimore, MD, US
BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people's health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 29,000 associates in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public.

About us

Description

Technical Leader in computational mechanics to design and drive CAE initiatives for medical device packaging for multiple product platforms.

The candidate will be the Technical Lead on ongoing initiatives toward building deep computational expertise within packaging R&D organization, which is accountable for designing & developing complete packaging solutions for new and existing medical devices from all product platforms within BD Medical Surgical Systems. Specific responsibilities will include (but not limited to) the following:

* Lead / perform CAD/CAE modeling / analyses for rigid/ flexible plastic/paper components
* Enhance CAE competencies within the group by identifying opportunities and implementing solutions
* Engage corporate R&D, materials R&D to identify & leverage synergies
* Develop and validate (per design control requirements) packaging components, designs and processes/technologies for various sterilization modes preserving the safety and efficacy over the shelf life
* Translate customer/user, marketing, regulatory, medical requirements into specific, measurable functional performance
* Evaluate new packaging concepts, technologies, test methods using engineering first principles
* Create prototypes, drawings, specifications, test instructions
* Perform root cause analysis for field, plant concerns, as needed
* Demonstrate strong accountability for successful completion of designated tasks
* Proactively develop, maintain & share technical knowledge in specialized area(s), remaining up-to-date on current trends and best practices. Actively coach junior associates and promote learning
* Provide Project Leadership to cross-functional teams comprising QA, MA, RA, Mktg, Mfg
* Effectively lead and direct the work of other engineers and laboratory technicians
* Ensure compliance with BD quality policies, procedures and practices as well as with all local, state, federal and BD safety regulations, policies and procedures

Qualifications

* Ph.D. in Mechanical/Chemical/Biomedical/Polymers or related technical field with a minimum 2 years relevant experience.
* Design for Six Sigma preferred
* Demonstrated experience in building and validating (on a physical application) computational mechanics models for rigid & flexible materials (plastic/paper)
* Demonstrated experience leading and completing projects meeting time, quality commitment
* Designing, developing, analyzing experiments
* Experience with package processing equipment & process development, preferred
* Experience leading Six Sigma (DFSS) projects preferred
* Computational structural and fluid mechanics
* 3D CAD modeling
* Understanding of disciplined product development processes & methods
* Excellent cross-functional influencing skills
* Strong sense of accountability
* Must be comfortable making practical assumptions with engineering justifications, where needed
* Understands the cost/benefit of experiments/analyses
* Design and statistical analysis of experiments
* Project planning
* Working knowledge of ISO, FDA and international regulatory and quality requirements applicable to medical device packaging preferred

Job
Mechanical Engineering

Primary Location
US-New Jersey-Franklin Lakes

Shift
First Shift / Day Job

Relocation Available
Yes]]>http://www.bd-careers.com/job/FRANKLIN-LAKESSHIFTFIRST-SH-Principal-Engineer-Job/709251/7092517092512010-04-10BDfull-timeUSDstarting0BS