FUJIFILM Healthcare Americas Corporation is seeking a Complaint Handling professional to ensure ongoing compliance with U.S. FDA medical device regulations, ISO 13485, and related standards.
The role involves evaluating complaints, coordinating with Quality, Regulatory Affairs, and Corporate teams, and driving CAPA activities to maintain quality records. The ideal candidate has 3+ years of FDA-regulated quality system experience, strong knowledge of global medical device standards, and excellent
#J-18808-LjbffrQuality & Regulatory Complaint Specialist in twinsburg at Unknown Company
This position is listed as full time and onsite.