Hybrid Global Regulatory Affairs Specialist, Medical Devices
Arrotek Medical Ltd
Theragenics, the parent company behind Arrotek, seeks a Regulatory Affairs Specialist to drive global regulatory compliance and submissions for medical devices across domestic and international markets. You will collaborate with Quality, Engineering, Operations, and Documentation teams to manage FDA 21 CFR 820, ISO 13485, EU MDR, and regulatory filings, ensuring timely approvals and ongoing compliance in a hybrid role. #J-18808-Ljbffr Arrotek Medical Ltd
Vacancy posted 2 days ago
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