Senior Technical Writer 3065677 I.Html

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