Technical Writer

We anticipate the application window for this opening will close on - 31 Oct 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 The Technical Writer will develop complex technical materials (labeling) that instruct users in the safe and proper use of Medtronic Neuromodulation products and therapies. The audiences for these materials include physicians, nurses, hospital technicians, and patients.                     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. • Simultaneously manage up to two labeling updates and one small, new-product-introduction project that involves multiple labeling pieces. • Understand and adhere to all quality management system documents and product commercialization procedures applicable to labeling development. • Research and write requirements used to create labeling content, and write requirement trace reports. • Assist in providing documentation for CAPAs, and departmental and business-unit audits. • Contribute to time and cost estimates for labeling deliverables for project teams. • Develop illustrations in cooperation with professional illustrators. • Participate on department and business-unit initiatives. • Oversee Engineering Change Order process for labeling, including writing change control plans and presenting to the Change Control Board. • Coordinate translations with Medtronic Translations and track the status of translations. • Prepare and occasionally present documentation for product issue escalation events, deviations and functional reviews. • Complete labeling proofs, develop documentation for regulatory submissions, and carry out other tasks as assigned. Must Have: Minimum Requirements                                                                  • Bachelor’s degree required • Minimum of 2 years of relevant experience, or advanced degree with a minimum of 0 years of relevant experience. Nice to Have • MA/MS in Communications, English, Journalism, or Scientific/Technical Communications. • 2+ years of job-related experience. • Experience developing technical manuals in a regulated environment. • Cross-functional project management experience. • Experience working in an engineering environment. • Experience writing in XML publishing systems. • Experience interpreting international standards. • Experience with writing for translations in an international organization. • Experience working with human factors and involvement with human factors studies. • Experience with writing manuals for complex hardware and software systems. • Coursework or experience working in the fields of graphic design, human factors, electronics, biology, anatomy, or physiology. • Experience working with manufacturing documentation and product-lifecycle systems. • Experience working in a highly regulated environment. • Experience working for a medical device or pharmaceutical company. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed