Medical Device Software Quality Engineer – Regulatory & V&V
Listed on 2026-09-17
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Software Development
Software Testing
Philips is hiring a Software Design Quality Engineer in Bedford, MA for an on-site, full-time role. You will lead software design assessment, verification, and validation activities to ensure safety, quality and regulatory compliance throughout the lifecycle.
You will drive risk management (ISO 14971), traceability, cyber security risk management, and post-market analytics. A bachelor’s degree and strong communication skills are required; salary ranges reflect market at Bedford, MA.
Join us at Mass Digital Health as our next Medical Device Software Quality Engineer – Regulatory & V&V in MA, United States.
This opportunity is part of our work in IT & Technology.
The advertised compensation is 102..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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