Global Regulatory & Quality Lead for Medical Devices

A leading medical device firm located in Minnesota is seeking a detail-oriented Quality & Regulatory Specialist to support compliance and quality management efforts. You will lead regulatory affairs, maintain the Quality Management System, and collaborate with various teams to ensure adherence to international regulations and standards. The ideal candidate should have 5-8 years of industry experience and strong knowledge of relevant medical device regulations. This role offers the opportunity to make a significant impact in a dynamic environment. #J-18808-Ljbffr