EU Regulatory Strategist: IVDR Writing & Submissions

A leading medical device firm located in South Portland, Maine, seeks a Regulatory Specialist to oversee technical writing and regulatory strategies for In Vitro Diagnostic products. The role involves supporting product development, managing submissions, and ensuring compliance with EU regulations. Ideal candidates should have experience in regulatory affairs, particularly with IVDR, and strong analytical skills to navigate the complexities of medical device regulations. #J-18808-Ljbffr