At Medtronic you can begin a life-long 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, compassionate world.

**A Day in the Life**
Supporting Design and Development Control activities with regulatory requirements, direction, tactics and strategies and working in a team environment with all organizational departments. Preparation of document packages for international regulatory submissions from all areas of company, internal audits and inspections.

**Responsibilities may include the following and other duties may be assigned:**

+ Prepare, review, file, and support premarket documents for global registrations for assigned projects.
+ Collaborate with business unit and international regulatory affairs personnel to support marketing authorizations for assigned projects.
+ Review pre-clinical, and clinical protocols and as...