Global Regulatory Affairs Specialist for MDR/IVD

An established industry player is on the lookout for a Regulatory Affairs Specialist 2 to join their dynamic team. This role is pivotal in ensuring compliance with international regulations for IVD medical devices, requiring a blend of technical expertise and project management skills. You will be responsible for preparing submission dossiers, interacting with regulatory agencies, and supporting new product development. If you thrive in a fast-paced environment and have a strong background in regulatory affairs, this is an exciting opportunity to make a significant impact in the medical device industry. #J-18808-Ljbffr