Global Regulatory Affairs Specialist - Medical Devices
Actalent
Actalent in Huntersville, NC seeks a Regulatory Affairs Specialist to execute regulatory strategies that support registration and lifecycle management of medical devices. You will navigate FDA and international requirements, manage submissions, and collaborate with Quality, R&D, and manufacturing to ensure compliant product lifecycle. The role requires at least 3 years in regulatory affairs for medical devices, with EU MDR and 21 CFR Part 820 experience. #J-18808-Ljbffr
Vacancy posted 1 day ago
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