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Global Regulatory Affairs Specialist - Medical Devices

Jobtailor

Jobtailor in Colorado is seeking a Regulatory Affairs professional to support medical device submissions and lifecycle management. You will coordinate document packages for FDA and international submissions and interact with notified bodies while ensuring compliance with EU MDR, MDD, and ISO standards. The role requires a bachelor’s degree, 2+ years of regulatory experience (or advanced degree), and U.S. work authorization. RAC progress is a plus and collaboration across teams is essential. #J-18808-Ljbffr

Vacancy posted 4 days ago
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