EMEA Regulatory Affairs Specialist — Medical Devices

Integra LifeSciences Corporation is looking for a Regulatory Affairs Specialist EMEA in Saint-Priest. The role involves coordinating product registrations, supporting market access, and ensuring compliance with regulations throughout EMEA.

The ideal candidate must have a background in pharmaceuticals or medical devices and at least 3 years of relevant experience. Strong project management skills and fluency in English are required. Join us to contribute to the future of healthcare.