Senior Technical Writer

Job Summary

Supporting a global LabVantage LIMS implementation, the remote contract Senior Technical Writer will author, revise, and manage GMP documentation, leveraging AI tools to enhance document generation and ensure compliance and inspection readiness.

Key Responsibilities

• Author and revise GMP documentation (SOPs, forms, job aids, validation evidence) for LabVantage deployment
• Leverage AI tools to accelerate document drafting, review cycles, and testing coverage
• Coordinate with QA, QC, IT, and document control teams to ensure inspection-ready content

Required Qualifications

• 5+ years of technical writing experience in GMP-regulated pharma or biotech environments
• Hands-on experience authoring SOPs, validation documentation, and regulated technical content
• Experience using AI tools (Claude, Copilot, or similar) to improve documentation efficiency
• Strong knowledge of document control, compliance, and inspection readiness