Requirements: English
Company: Barrington James
Region: Dijon , Bourgogne-Franche-Comt
This is a fantastic opportunity to be part of an innovative company that is committed to delivering high-quality medical devices to the market. As a Regulatory Affairs Officer , you will be responsible for ensuring compliance with medical device regulations and standards . Ensure compliance with EU MDR, ISO 13485, FDA regulations , and other international requirements. Masters degree in Quality/Regulatory Engineering, Biomedical Science, or a related field . &##3+ years of experience in Regulatory Affairs within the medical device industry . Strong knowledge of medical device regulations , including EU MDR, ISO 13485, FDA 21 CFR 820, and international standards . Work with cutting-edge medical technologies that make a real impact on patient lives. &##