Technical Writer

📋 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.