We anticipate the application window for this opening will close on - 19 Jan 2026 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 Sitting in the Diabetes Regulatory Operations Team, the Regulatory Operations Specialist will be a key member managing regulatory data attributes, distribution control mechanisms, and preparation and publishing of submissions. This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care. The successful candidate will: Have a background working within a Quality System Work cross-functionally and in a matrixed environment Manage multiple projects, prioritizing work based on criticality Have experience with FURLs and UDI data Have experience with and participate in continuous improvement activities Have experience with Regulatory Information Management (RIM) System A Day in the Life Develop key partnerships with stakeholders across functional groups, and regions to align on harmonized processes Manage publishing activities for multiple projects Manage UDI Database including uploading of data to relevant regulatory bodies Manage FURLs Database including uploading of data Support Product Blocks and Product Release Activities
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees