Regulatory Affairs Coordinator
Medasource
Medasource is seeking a regulatory support specialist for a Fortune 500 medical technology client in Raritan, NJ. This contract role (6 months to 1 year) involves preparing and submitting FDA CFG requests and coordinating regulatory documentation for international registrations. You will ensure accuracy, manage document routing for signatures, oversee notarization and apostille where needed, and maintain traceability of regulatory data while supporting cross‑functional teams. #J-18808-Ljbffr
Vacancy posted 2 days ago
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