Regulatory Affairs Specialist - Medical Devices
Merck & Co.
Fujifilm Healthcare Americas Corporation is seeking a Regulatory Affairs professional to ensure ongoing compliance with US FDA medical device regulations and ISO 13485 across multiple regions. You will collaborate with engineering, quality, regulatory, and service teams to prepare submissions, maintain documentation, and support post-market activities. The role requires a bachelor’s degree and 2+ years in FDA-regulated environments or RAC with 4+ years of experience. #J-18808-Ljbffr Merck & Co.
Vacancy posted 1 day ago
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