IVDR Regulatory Strategy Specialist II – Medical Devices

A leading recruitment firm is seeking a Regulatory Affairs Specialist II to ensure compliance with EU regulatory requirements for medical devices. This role involves preparing technical documentation for international product registrations and providing regulatory support throughout product development. Candidates should possess a Bachelor’s degree and have at least 4 years of experience in a regulatory affairs role. Strong knowledge of IVDR is essential, along with excellent communication skills. This position is based in South Portland, Maine. #J-18808-Ljbffr