Contract Medical Device Regulatory Engineer

Myn is seeking a Regulatory Affairs Engineer for a contract role in Cambridge to bridge engineering and regulatory oversight. You will build and maintain technical files and ensure products meet UK MDR 2002, UKCA and EU MDR/IVDR requirements throughout their lifecycle.

You will collaborate with design, quality and regulatory teams, provide input for design changes and risk management, and liaise with MHRA, notified bodies and test labs as required.

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