Senior Global Medical Device Regulatory Specialist
Sonova Group
Sonova Group is seeking a Senior Specialist in International Regulatory Affairs to support global regulatory activities for Class III medical devices. This role is essential for obtaining and maintaining regulatory approvals across international markets, coordinating with local teams, and ensuring compliance with global regulations. The ideal candidate will have experience in pre‑market and post‑market regulatory affairs, possess strong writing skills, and be familiar with global regulations. A Bachelor's degree and a proactive approach to managing multiple tasks are required. #J-18808-Ljbffr Sonova Group
Vacancy posted 3 days ago
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