Regulatory & Compliance Project Lead (Medical Devices)

Nemera France SAS seeks a Regulatory & Compliance Project Manager to lead regulatory activities for their medical devices. The successful candidate will have a strong engineering background, at least 5 years of experience, and knowledge of regulatory compliance processes.

You will collaborate with various teams to ensure adherence to standards and regulations while supporting product-specific interactions with stakeholders. Fluent English is required, and the role is based in Lyon, France.