GXPeople Global Ltd. in London is seeking a Regulatory Affairs Manager for medical devices who will own regulatory strategy from day one, including US FDA submissions and EU MDR planning.
The role leads the FDA 510(k) process, coordinates engineering CROs and test houses, and builds post-market processes such as registration, UDI/GUDID and recalls. You will influence growth and work directly with the CEO in a fast-moving team.
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Regulatory Affairs Manager, Medical Devices – FDA 510(k) Lead in City of London employer: GXPeople Global Ltd.
GXPeople Global Ltd. is an exceptional employer that fosters a dynamic and innovative work culture in the heart of London, offering employees the chance to make a significant impact in the medical devices sector. With a strong emphasis on professional growth, equity incentives, and a collaborative environment, team members are encouraged to develop their skills while contributing to cutting-edge projects. Join us to be part of a fast-paced startup atmosphere where your contributions are valued and rewarded.
