Regulatory Affairs Specialist
FUJIFILM Corporation
Fujifilm Healthcare Americas Corporation is seeking a Regulatory Affairs professional to support full compliance with US FDA medical device requirements, ISO 13485, and applicable laws. The role involves preparing 510(k)/PMA submissions, EU Technical Documentation, and international filings while collaborating with QA, R&D, service, and regulatory teams. Ideal candidates have a BS in a related field and 2+ years of RA experience in a FDA-regulated environment, with RAC preferred. #J-18808-Ljbffr
Vacancy posted 16 hours ago
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