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At Medtronic, you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. As a Technical Writer, you will support the production of customer-facing product documentation, including but not limited to: user's guides, service manuals, 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 R&D new product development as well as sustaining activities/legacy document maintenance for various products produced by the Medtronic Neuroscience portfolio. You will collect inputs from cross-functional technical staff to gather data for documentation, as well as research and translate technical information into manuals and/or web-based documents for nontechnical and technical users. You will be responsible for supporting documentation to the customer-facing literature which may include labeling design plans, trace documents, technical reviews, and verification deliverables. Additionally, you will support product documentation updates to comply with EUMDR, FDA, and other regulatory body requirements by incorporating customer inputs and ensuring standardization of document development to comply with Medtronic design standards. In this role, you will manage all aspects of document development and assist in production release, including draft reviews and formal labeling approvals, coordination of translations, and initiating CO/CA release. You will revise, edit, and format legacy product documentation as required, ensuring compliance of labeling with all applicable regulatory/QSR requirements. You will create, edit, and format documentation as part of the compliance with requirements from the European Union (EU Medical Device Regulation). Effectively managing multiple projects, changes in project scope, and shifting priorities will be essential to maintain project requirements and ensure deadlines are met. Collaboration with departmental and cross-functional peers will be crucial to ensure proper resolution to questions and issues during the document development process. Continually reviewing the document development process to ensure quality in labeling output will be a key responsibility.
