Global Regulatory Affairs Specialist - Medical Devices
Sakura Finetek
Sakura Finetek USA, Inc. is seeking a Regulatory Affairs Specialist in Torrance, CA. You will guide regulatory submissions for domestic and international markets and work with Quality, Engineering, R&D, and Sales to ensure compliant product lifecycle management. The role emphasizes meticulous regulatory analysis, adherence to QSR/ISO requirements, and proactive interaction with regulatory bodies. Collaboration across departments is essential to drive timely approvals. #J-18808-Ljbffr
Vacancy posted 1 day ago
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