R&D Engineer III New Haven, CT

The Engineer III R&D assists in the research design and development of novel medical devices through assessment of clinical needs concept design engineering analysis implant characterization specification development and verification / validation testing. This individual works cross-functionally with Marketing Operations Quality Supply Chain and external partners to ensure successful project execution.

A successful individual must understand good design and experimental principles engineering concepts and be able to solve complex problems in a team environment.

Key Duties & Responsibilities :

• Serve as technical lead for new product development identifying project requirements and leading execution of design control activities from concept through commercial launch and design transfer
• Identify user needs and technical specifications by collecting surgeon feedback (VOC) conducting labs and observing surgeries
• Develop innovative solutions to complex design challenges while balancing performance cost and manufacturability.
• Plan and execute design verification and validation testing using statistical rationale for planning and analysis of results
• Solve technical challenges by performing root cause analysis design of experiments writing and executing protocols and technical reports
• Plan coordinate and execute changes to product or manufacturing processes to support new requirements additions and improvements
• Plan and conduct product testing in clinically relevant setups including benchtop biomechanical and ex-vivo cadaver
• Support commercial Marketing and Sales teams by providing technical expertise and training on products
• Partner with Quality and Regulatory teams to ensure compliance with customer industry and regulatory requirements (ISO FDA etc. if applicable).
• Support Supply Chain by evaluating suppliers reviewing tooling concepts and resolving technical issues.

Minimum Requirements :

Preferred Requirements :

Other Attributes :

This position is not eligible for employer based sponsorship. Disclosure as required by applicable law the annual salary range is . The actual compensation may vary based on geographic location work experience education and skill level. The salary range is CONMEDs good faith belief at the time of this posting

Benefits :

CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.

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CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights : Workplace Discrimination is Illegal Poster reaffirms this commitment.

Colorado Residents : In any materials you submit you may redact or remove age-identifying information such as age date of birth or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

If you feel you need a reasonable accommodation pursuant to the ADA you are encouraged to contact us at option #5.

Key Skills

Laboratory Experience,Vendor Management,Design Controls,C / C++,FDA Regulations,Intellectual Property Law,ISO 13485,Research Experience,SolidWorks,Research & Development,Internet Of Things,Product Development

Employment Type : Full-Time

Experience : years

Vacancy : 1