IVDR Regulatory Affairs Specialist II – Hybrid Contract

A staffing and consulting firm is seeking a Regulatory Affairs Specialist II to support the transition to EU’s In Vitro Diagnostic Regulation (IVDR). This hybrid role involves revising technical documentation, updating labeling, and coordinating regulatory notifications. Candidates should have a Bachelor's degree and 3–5 years of relevant experience in the IVD industry. Excellent communication skills and the ability to work both independently and in teams are essential. Join us to ensure critical compliance with evolving regulations. #J-18808-Ljbffr