Regulatory Affairs Lead – Medical Devices (UKCA/CE MDR)

A leading medical device manufacturer in Northallerton is seeking a regulatory lead to ensure compliance with UKCA and CE marking requirements. This role involves working cross-functionally with teams across Quality, R&D, and Operations to maintain compliant documentation and support market access. The ideal candidate is ambitious and independent, eager to contribute to innovative projects. Apply quickly as the recruitment process may close prematurely. #J-18808-Ljbffr