Staff Mechanical Design Engineer

The Staff Mechanical Design Engineer will focus on the design of advanced diabetes care products. The products will bring new capabilities and technologies to the treatment of diabetes.
Duties and Responsibilities:
Innovate and define technical solutions for design problems and lead efforts to realize the technical solutions
Design, prototyping and testing of new products
Improve and incorporate novel features into existing products. Confirm product capabilities by designing feasibility and testing methods and systems
Use first principles and advanced engineering methods to guide the development process
Perform 3D modeling and tolerance analysis and apply DFSS tools as appropriate
Design for Manufacturing/Assembly (DFM)
Interact with vendors to understand effect of materials, process, advanced capabilities, etc. on design decisions and product performance
Conduct and participate in design reviews, DFMEA's, and other design documentation as needed
Design fixtures for assembly, testing and inspection
Write, implement and lead design verification protocols and activities
Participate in interactions with customers and health care providers
Comprehend and interpret their needs and requirements correctly and transfer into novel product designs effectively
Contribute to R&D functional planning, budgeting, and tracking
BS in mechanical engineering, MS preferred
Minimum of 8 years experience as a mechanical designer/ engineer in medical device industry
Experience in Diabetes Care Infusion Systems and/or medical devices disposables
Additional and Preferred Qualifications:
Proficient in Pro/E and/or SolidWorks and GD&T
Advanced knowledge of engineering first principles
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
"Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status."

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