Regulatory Affairs Program Lead – Medical Devices

NEMERA in Lyon is seeking a Regulatory Affairs Project Manager (F/M/X) responsible for leading regulatory design projects for drug delivery devices. You will interact with cross-functional teams to ensure compliance with regulatory requirements.

The ideal candidate has an engineering degree, at least 5 years of experience in the medical devices industry, and knowledge of regulatory standards. NEMERA values diversity and inclusion, providing an equitable work environment.