Regulatory Affairs Specialist — Medical Devices
Listed on 2026-10-09
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Healthcare
Healthcare Compliance
FUJIFILM Healthcare Americas Corporation is seeking a Regulatory Affairs professional to ensure ongoing compliance with US FDA medical device regulations, ISO 13485, and other applicable standards. This role supports registrations, submissions, and documentation across global markets.
You will collaborate with R&D, quality, and operations to prepare 510(k) and PMA filings, maintain EU MDR documentation, and manage post-market surveillance activities.
As a Regulatory Affairs Specialist — Medical Devices, you will play an important part at Fujifilm in Providence, RI, United States.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Providence, RI, United States.
This opportunity is part of our work in Legal, Management & Operations.
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