Remote Regulatory Affairs Specialist (Medical Devices)

FUJIFILM Healthcare Americas Corporation is seeking a Regulatory Affairs professional to ensure ongoing compliance with U.S. FDA medical device regulations and ISO 13485 standards. The role involves submissions, documentation, and cross-functional collaboration to support product life‑cycle activities. The ideal candidate has a bachelor’s degree in a related field, 2+ years in U.S. FDA regulated Regulatory Affairs (or 4+ years with RA certification), and broad knowledge of global medical device #J-18808-Ljbffr FUJIFILM Holdings America Corporation