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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, requ
Easy Apply
Full-time
Depends on Experience