Medical Device Software Quality Engineer – Regulatory & V&V
Listed on 2026-10-02
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Engineering
Biomedical Engineer, Quality Engineering
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.
We would love to welcome a new Medical Device Software Quality Engineer – Regulatory & V&V to our team in MA, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Medical Device Software Quality Engineer – Regulatory & V&V role in the description above.
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