Global Regulatory Affairs Specialist - Medical Devices
Listed on 2026-09-22
-
Healthcare
Healthcare Compliance, Medical Science Liaison
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.
For the Global Regulatory Affairs Specialist
- Medical Devices position at Jobtailor, we are reviewing applications now.
We are currently recruiting a Global Regulatory Affairs Specialist
- Medical Devices for our team in CO, United States.
This is a genuine position to take on the Global Regulatory Affairs Specialist
- Medical Devices role at Jobtailor.
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