Technical Writer

Overview Technical Writer, Medical Devices — 12-month contract. Onsite in Sunnyvale, CA. Be among the first to apply. Responsibilities Plan, write, and edit Instructions for Use (IFUs) for medical device systems and instruments, including system manuals, instrument manuals, and ship-with literature using Adobe FrameMaker, Adobe InDesign, or XML. Collaborate with team members and cross-functional Subject Matter Experts (SMEs) to research, develop, and validate content. Own document creation from inception to completion. Ensure compliance with FDA and other regulatory guidelines. Partner with designers and technical illustrators to develop documentation images (raster and vector). Conduct validation and verification of technical documentation. Manage documentation control steps to release final documents. Participate in product development core teams as a representative for technical publications. Required 5–8 years of technical writing experience in hardware, software, biotechnology, or medical environments, including documentation for highly technical audiences. Strong experience with authoring tools: Adobe FrameMaker, Adobe InDesign, and Adobe Acrobat (preferred). Strong writing, grammar, and communication skills with the ability to communicate complex scientific and engineering concepts clearly. Familiarity with XML, Darwin Information Typing Architecture (DITA), and content management systems (strongly preferred). Ability to troubleshoot moderate FrameMaker and InDesign issues, update/improve document templates, troubleshoot online help software, and create error-free PDFs. Seniority level Mid-Senior level Employment type Contract Job function Writing/Editing and Other Industries Medical Equipment Manufacturing Hospitals and Health Care Biotechnology Research Referrals increase your chances of interviewing at GForce Life Sciences by 2x #J-18808-Ljbffr GForce Life Sciences