Regulatory Affairs Specialist – Medical Devices
Listed on 2026-10-09
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Healthcare
Healthcare Compliance, Medical Science Liaison
Fujifilm Healthcare Americas Corporation seeks a Regulatory Affairs professional to ensure FDA and ISO 13485 compliance for medical devices in the U.S. and abroad. You will manage registrations, prepare submissions, and advise design teams on regulatory strategies.
Responsibilities include EU/ international submissions, post-market activities, trend analysis, and collaboration with Quality, R&D, and Customer Service. A bachelor’s degree and 2+ years in FDA-regulated settings or RAC are required.
We have an opening for a Regulatory Affairs Specialist – Medical Devices in Bismarck, ND, United States within Legal, Management & Operations.
The following opening is for a Regulatory Affairs Specialist – Medical Devices with Fujifilm.
Our team is growing, and we are hiring a Regulatory Affairs Specialist – Medical Devices in Bismarck, ND, United States.
This Full Time opening is for the Regulatory Affairs Specialist – Medical Devices role at Fujifilm.
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