Senior quality engineer for medical device software with regulatory oversight responsibilities.
Lead technical quality initiatives across medical device software products, including SaMD, cloud-connected, and AI/ML solutions. Engage early in development to identify risks, influence architecture decisions, and ensure compliance with FDA and IEC standards. Partner with engineering teams on requirements, design reviews, and release readiness while maintaining independent quality judgment. Requires deep SDLC knowledge, code review capability, and experience with modern DevOps and testing practices.
Membership is €29/month, cancel anytime: every rate, every original listing link, and a daily alert for roles matching your filters.
Found at a specialist agency · listed 2 October 2026 · InsideJobs links you to the original posting.