Global MDR Regulatory Affairs Specialist (Medical Devices)

Academic Work is seeking a Regulatory Affairs Specialist located in Etoy, Switzerland. The candidate will oversee regulatory compliance and the product lifecycle of medical devices, ensuring adherence to international regulations while collaborating with R&D and Marketing teams globally.

Key responsibilities include submitting regulatory dossiers, managing product lifecycles, and ensuring documentation meets Medical Device Regulation standards. The ideal candidate has experience in regulatory affairs within the medical device industry and is available immediately.