Technical Writer/Document Analyst - Ranger Technical Resources
Technical Writer/Document Analyst #2557 Position Summary: Our partner, a global medical device manufacturer operating in a highly regulated industry, is seeking a Technical Writer/Document Analyst to support critical compliance documentation updates. As Analyst, you will be responsible for reviewing and redlining SOPs, design control documents, and device overviews to ensure they remain accurate, consistent, and audit ready. The scope includes core files tied to FDA design control changes, requiring precise updates that withstand regulatory scrutiny. Within this opportunity, you must thrive in a task-driven environment, focusing on disciplined execution and meticulous attention to detail. The ideal candidate brings experience in medical device documentation, regulatory standards, and document control practices, with a proven ability to maintain quality and consistency at scale. Experience and Education: BS in Computer Science, Information Technology, Arts or equivalent experience/field 5+ years in medical device, life sciences, or regulated manufacturing documentation Prior experience with FDA quality system regulations and design controls Work in regulated industries requiring structured documentation (e.g., medical devices, pharma, biotech) Background updating SOPs, device instructions, and controlled documents Familiarity with redlining and structured document review processes Track record of producing compliant technical documentation in highly regulated settings Skills and Strengths: