Technical Writer
EurofinsJob Description
📋 Description Develop, review, and maintain controlled docs for validation and lab operations. Ensure SOPs, forms, protocols are accurate, clear, and compliant. Collaborate with cross-functional SMEs to manage documents and quality initiatives. Write and edit forms, protocols, reports, and procedures from templates under supervision. Analyze documents to maintain style and content continuity. Update and revise technical documents as instructed. 🎯 Requirements Bachelor’s degree in medical laboratory sciences, biology, chemistry, or related scientific discipline. Additional education/training in technical, scientific, medical, or regulatory writing preferred. Minimum 2+ years of scientific/technical writing experience preferred. In lieu of writing experience, 4+ years in regulated clinical lab or regulatory affairs/QA accepted. Knowledge of GDP and regulated environments (CLIA, CAP, GLP) preferred. Authorization to work in the United States without sponsorship. 🎁 Benefits Excellent full-time benefits including medical, dental, and vision. Life and disability insurance. 401(k) with company match. Paid vacation and holidays.