Regulatory Affairs Specialist
Actalent
Actalent in Raleigh, NC seeks a Regulatory Affairs Specialist to execute established regulatory strategies that support registration and lifecycle management of medical devices. You will navigate FDA and international requirements, coordinate submissions, and communicate with cross-functional partners to drive timely regulatory decisions. In this permanent, onsite role, you will lead change controls and labeling reviews in the first six months, support EU MDR activities, and collaborate with #J-18808-Ljbffr
Vacancy posted 8 hours ago
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