Design Quality Engineer – Med Device, Hybrid
Listed on 2026-11-04
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Engineering
Quality Engineering, Biomedical Engineer, Regulatory Compliance Specialist, Medical Device Industry
Stryker is seeking a Staff Design Quality Engineer in Waltham, MA to support new product development and ensure quality across the medical device lifecycle. You will partner with R&D, Regulatory Affairs, Manufacturing, and suppliers to apply design controls, risk management, V&V, and ISO 13485 compliance.
This hybrid role requires a Bachelor's degree in engineering and at least four years in Quality Engineering, with knowledge of FDA 21 CFR Part 820, ISO 13485, and risk management.
We are currently recruiting a Staff Design Quality Engineer – Med Device, Hybrid for our team in Waltham, MA, United States.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Waltham, MA, United States.
This opportunity is part of our work in Engineering.
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