Global Medical Device Regulatory Affairs Specialist
Listed on 2026-10-06
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Healthcare
Healthcare Compliance, Medical Device Industry, Medical Science Liaison
Katalyst CRO is seeking an experienced Regulatory Affairs professional to drive submissions for U.S. and European medical devices. You will guide product development with regulatory input, coordinate inputs across R&D, Quality, Medical, and Manufacturing, and ensure compliance with 21 CFR 820 and ISO 13485.
The ideal candidate holds a B.S. in life sciences or engineering, 2–5 years of device regulatory experience, RAC certification, knowledge of 510(k) and EU MDR/MDD, plus strong communication
We are currently recruiting a Global Medical Device Regulatory Affairs Specialist for our team in Seattle, WA, United States.
As a Global Medical Device Regulatory Affairs Specialist, you will play an important part at Katalyst CRO in Seattle, WA, United States.
We invite applications for the Global Medical Device Regulatory Affairs Specialist position located in Seattle, WA, United States.
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