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Global Regulatory Affairs Lead - Medical Devices

Brio Group

Brio Group seeks a Regulatory Affairs Specialist to support regulatory strategy and compliance across the product lifecycle. You will collaborate with Engineering, Quality, Operations, and external consultants to ensure FDA and EU MDR readiness for both commercial products and new launches. You will mentor a junior specialist, help develop future regulatory talent, and manage multiple priorities while maintaining meticulous regulatory standards and timelines. #J-18808-Ljbffr

Vacancy posted 2 days ago
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