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For your reference, we have included the original job posting below.
Principal Engineer- Pen Injection Platform
Job Number:
25359210
Company Name:
Becton Dickinson
Job Location:
Franklin Lakes, NJ US
Job Category:
Engineering & Architecture
Principal Engineer- Pen Injection Platform
Principal Engineer- Pen Injection Platform-PRO10134
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 product development Engineer to join our R&D team. Working in an R&D team, the senior product development 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, R&D core team member 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 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.
Duties and Responsibilities:
* 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 * Design and develop in vivo and in vitro models to evaluate product features & improvements * Uses engineering first principals and advanced engineering methods to guide the development process * Perform 3D modeling and tolerance analysis * 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 medical devices disposables * Proficient in Pro/E and/or SolidWorks and * 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
