Neuro Regulatory Affairs Specialist Global Submissions

A leading global healthcare technology company is seeking a Regulatory Affairs Specialist in Minneapolis, MN to manage regulatory submissions for medical devices. The candidate should have experience in Class II and III devices and a strong understanding of FDA and EU regulations. This role involves working closely with engineers and regulatory agencies to ensure product compliance and successful market introduction, and offers competitive salary packages and benefits to foster employee well-being. #J-18808-Ljbffr