Technical Writer- LabVantage
Author and manage GMP documentation for LabVantage LIMS implementation
The Sr. Technical Writer supports a global LabVantage LIMS implementation by authoring, revising, and managing GMP documentation including SOPs, forms, job aids, and validation evidence. This role leverages approved AI tools such as Claude and Copilot to accelerate document generation, review, and testing while maintaining compliance and inspection readiness. The position is a remote consultant role focused on ensuring documentation meets regu...
Why This Role?
Leverage approved AI tools like Claude and Copilot to accelerate GMP documentation workflows
Key Responsibilities
- Author and revise GMP documentation such as SOPs, forms, and job aids
- Manage validation evidence for LabVantage LIMS implementation
- Use AI tools including Claude and Copilot to support document generation and review
- Ensure documentation maintains compliance and inspection readiness
- Support global LIMS implementation through technical writing tasks
Requirements
- Experience authoring GMP documentation including SOPs and validation evidence
- Familiarity with LabVantage LIMS or similar laboratory information systems
- Proficiency using AI tools such as Claude and Copilot for document workflows
- Ability to maintain compliance and inspection readiness in documentation
- Experience supporting global implementations in regulated industries
Required Skills
Keywords
View Original Description from Adzuna
Original description from Adzuna
Job: 3035848 Job Description: Role: Sr. Technical Writer- LabVantage Location: Remote Type: Consultant Summary: The Sr. Technical Writer supports a global LabVantage LIMS implementation by authoring, revising, and managing GMP documentation including SOPs, forms, job aids, and validation evidence. This role leverages approved AI tools, including Claude and Copilot, to accelerate document generation, review, and testing while maintaining compliance and inspection readiness. Key Responsibilities:…
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