Technical Writer: Medical Device Documentation (Contractor, Remote)

Technical Documentation Specialist Our rapidly expanding engineering team needs a detail-oriented and experienced technical documentation specialist located in St. Paul, MN. This is a contractor position that will be primarily remote, with occasional on-site meetings. Our company develops cutting-edge medical devices, and this role is critical to ensuring our products are safely and effectively used. Contribution Highlights Craft and maintain detailed technical documentation, including user manuals, installation guides, and troubleshooting guides for medical devices. Collaborate closely with engineers, product managers, and quality assurance teams to ensure accuracy and completeness of all documentation. Manage the documentation revision control process, ensuring proper versioning and archival of all documents. Conduct research and gather information from subject matter experts to create clear and concise explanations of complex technical concepts. Organize and structure information for optimal user experience, adhering to established documentation standards. Translate engineering specifications and product requirements into user-friendly content. Create visual aids, such as diagrams and flowcharts, to enhance understanding of technical concepts. Participate in documentation reviews to identify areas for improvement and ensure alignment with user needs. Manage multiple documentation projects simultaneously, meeting deadlines and maintaining high-quality standards. Adapt to changes in product specifications and incorporate updates into existing documentation. Required Attributes A proven background in technical writing, ideally within the medical device industry. Practical proficiency with documentation tools and software, such as Adobe FrameMaker, MadCap Flare, or similar. An unwavering commitment to accuracy and attention to detail. The ability to explain sophisticated technical details simply and effectively. Exceptional communication and interpersonal abilities, fostering productive collaboration with various teams. Solid experience with version control systems. Knowledge of regulatory requirements for medical device documentation. Familiarity with content management systems (CMS).Demonstrated project management skills. Comfort in a remote work environment, displaying self-discipline and organization. Our Benefits to YouWe appreciate our contractors and provide competitive hourly rates. We provide access to professional development opportunities. We value your expertise and offer a supportive and collaborative work environment. We prioritize a work-life balance that allows you to maintain well-being. We value open communication and feedback, creating a culture of continuous improvement.