Regulatory Affairs Lead – Medical Devices (MDR/FDA)

Elos Medtech AB is seeking a Senior Specialist in Regulatory Affairs for its site in Muntelier. The role focuses on managing regulatory strategy, ensuring compliance throughout the product lifecycle, and leading documentation efforts.

The ideal candidate will have a degree in Engineering, strong knowledge of European MDR and U.S. FDA regulations, and several years of experience in the medical device sector. The company promotes an open culture and offers excellent benefits.