Regulatory Affairs Specialist
Envista Holdings Corporation
Implant Direct, part of Envista Holdings, seeks a Regulatory Affairs Specialist to manage global regulatory submissions for medical devices from Thousand Oaks, CA. You will coordinate 510(k) filings, CE documentation, and international dossiers, working with cross-functional teams to ensure compliance and timely approvals. The role requires 3 years of medical device regulatory experience, strong documentation skills, and the ability to navigate regulatory authorities across multiple markets. #J-18808-Ljbffr
Vacancy posted 2 days ago
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