Senior Regulatory Affairs Lead, Class III Medical Devices
Listed on 2026-09-17
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Healthcare
Medical Device Industry, Healthcare Compliance
Bio Talent in Massachusetts is seeking a Senior Regulatory Affairs Specialist to lead and execute regulatory strategies for complex Class III medical devices, collaborating with Clinical, Quality, R&D and Manufacturing teams in a fast-paced, growth-oriented environment.
The role centers on leading FDA submissions (including PMAs), global registrations, and guiding design controls, risk management, and product commercialization throughout development.
We are looking to fill the Senior Regulatory Affairs Lead, Class III Medical Devices position at Bio Talent 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 Senior Regulatory Affairs Lead, Class III Medical Devices role in the description above.
We appreciate your interest in this position.
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