Role Overview At Medtronic, you can begin a lifelong career of exploration and innovation while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected and compassionate world. A Day in the Life - Coordinate and prepare documentation for regulatory submissions across the organization. - Oversee the compilation of materials for license renewals and annual registrations. - Recommend updates to labeling, manufacturing, marketing, and clinical practices to meet regulatory standards. - Monitor tracking systems and stay informed on regulatory changes. - Interact with regulatory agencies as needed. - Develop strategies for timely approval of clinical trial applications.