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Global Medical Device Regulatory Affairs Specialist
Job in
Saint Paul, Ramsey County, Minnesota, 55199, USA
Listed on 2026-08-30
Listing for:
Scanlan International
Full Time
position Listed on 2026-08-30
Job specializations:
-
Healthcare
Healthcare Compliance, Medical Science Liaison
Job Description & How to Apply Below
Scanlan International in Saint Paul, MN, is seeking a Regulatory Affairs Specialist to support market authorizations for medical devices across worldwide markets.
Responsibilities include maintaining US FDA registrations/listings, CE documentation, post-market surveillance, and post-delivery regulatory activities, with emphasis on accuracy and timely submissions. Bachelor’s degree and 1–3 years regulatory experience required;
Master’s in Regulatory Affairs preferred.
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