EU MDR Regulatory Affairs Consultant | Medical Devices

A reputable medical device manufacturer in Lyon is seeking an experienced Regulatory Affairs Consultant to support key projects over the next 12 months. This role involves leading the preparation and maintenance of regulatory submissions for EU MDR, managing updates to technical documentation, and advising internal teams throughout product development. The ideal candidate will have proven experience with EU MDR submissions, a strong background in medical devices, and excellent communication skills. This position offers a unique opportunity to play a crucial role in regulatory compliance. #J-18808-Ljbffr