Senior Regulatory Affairs Specialist – Medical Devices

A global medical technology firm located in Plymouth, Minnesota, seeks a Regulatory Affairs Support professional to assist in ensuring compliance with various regulations. The role includes preparing regulatory submissions, supporting project teams, and responding to customer queries. Ideal candidates will have a bachelor's degree and 3+ years of relevant experience in the medical device industry. Proficiency in regulatory databases and excellent communication skills are essential. #J-18808-Ljbffr