IVDR Regulatory Affairs Specialist - Hybrid

A leading medical technology company in Fort Worth seeks an Analyst to support the EU's In Vitro Diagnostic Regulation transition. Responsibilities include revising technical files, updating labeling specifications, and ensuring compliance with IVDR requirements. Candidates must have a Bachelor's degree in a relevant field and at least 3 years of experience in the IVD industry. Strong communication and analytical skills are essential. This is a 12-month hybrid contract position with a competitive hourly rate. #J-18808-Ljbffr