Technical Writer

We anticipate the application window for this opening will close on - 1 Aug 2026   Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life Our Cardiovascular Portfolio operating units offer devices and therapies that treat patients with abnormal heart rhythms and heart failure, peripheral, coronary, and aortic arterial diseases, and host of other cardiac and blood flow-related ailments. Together, we will transform the lives of people who suffer from these diseases. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.  This position will be based in Mounds View, MN.                     In this exciting role as a  Technical Writer , you will produce customer-facing product documentation, including but not limited to user guides and instructions for use (IFUs). This includes labeling for both clinicians and patients that  accompany  medical device products   that conform to the Medtronic documentation and quality assurance standards. Projects include new product development as well as sustaining activities/legacy document maintenance for various products produced by the Cardiovascular portfolio.     You will  identify  document requirements, collect inputs from cross-functional technical staff ,  and distill this technical information into detailed,  accurate  content for manuals and/or web-based documents for technical and non-technical users.     Responsible for supporting documentation to the customer-facing content which may include labeling design plans, trace documents, technical reviews, and  verification  deliverables. You will support product documentation updates to  comply with   regulations and international standards   by incorporating customer inputs and ensuring standardization of document development to  comply with  Medtronic design standards.     Role and Responsibilities   Responsibilities   may include the  following  and other duties may be assigned.   Plan, research, develop, and write medical device labeling, and manage labeling deliverables as part of cross-functional project teams under general supervision.   Write clear, simple content that speaks to customers in their own language. Understand the impact of localization on English content and writing for a global audience.   Effectively communicate the  appropriate level  of detail based on technical and customer requirements.   Collaborate openly and effectively with a range of stakeholders, including writers and subject matter experts.   Coordinate IFU release in the Product Lifecycle Management System ( Windchill and Azure DevOps ).   Understand how regulations, laws, and standards influence content design.   Understand and adhere to all quality management system documents and product commercialization procedures applicable to labeling development.   Manage multiple projects and communicate status proactively. Successfully negotiate project schedules, plans, and milestones.   Contribute to   time and cost estimates for labeling deliverables for project teams.   Take  direction  to be able to work independently and make sound decisions. Express ideas clearly and diplomatically.   Develop documentation for regulatory