Senior Regulatory Affairs - Medical Devices (Hybrid)
Sonova Group
Sonova is seeking a Senior Specialist, Regulatory Affairs in Valencia, CA. This hybrid role supports product approvals and registrations across international markets, with emphasis on APAC regulatory requirements for Class III devices. The position emphasizes regulatory submissions, lifecycle management, and collaboration with Quality, Clinical, and Development teams to ensure compliance and timely market access. #J-18808-Ljbffr Sonova Group
Vacancy posted 23 hours ago
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