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-LjbffrRegulatory Affairs Specialist – Medical Devices in Remote at Unknown Company
This position is listed as full time and onsite.