Regulatory Affairs Specialist, Medical Devices (EU MDR)

A global healthcare technology leader is seeking a Principal Regulatory Affairs Specialist for their Diabetes division in Greater London. This role involves coordinating regulatory submissions, leading compliance activities, and ensuring adherence to regulatory requirements. Candidates should have a strong background in medical device regulatory affairs, including UK MHRA submissions and CE/UKCA marking. The position offers competitive salary and benefits, contributing to healthcare innovation and equity. #J-18808-Ljbffr