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.
Step into the Regulatory Affairs Specialist — Medical Devices role at Fujifilm in Providence, RI, United States and grow with us.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 74.000 - 91.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Regulatory Affairs Specialist — Medical Devices role in the description above.
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