LabVantage LIMS Validation Specialist

Job Summary

A company is looking for a LabVantage LIMS Validation Specialist to lead the documentation and validation of LabVantage LIMS projects in a GxP regulated environment.

Key Responsibilities

• Lead the end-to-end documentation and validation processes of LabVantage LIMS in a GxP-regulated laboratory environment
• Author and maintain Design Specifications, ensuring alignment with regulatory and business requirements
• Develop and execute validation protocols (IQ/OQ/PQ) and ensure compliance with GMP, GLP, and GCP standards

Required Qualifications

• 5+ years of experience validating LabVantage LIMS in a GxP environment
• Strong expertise in CSV/Lab Systems Qualification document/deliverable authoring
• Experience with ValGenesis or similar validation lifecycle management tools
• Solid understanding of GxP, 21 CFR Part 11, and Data Integrity compliance requirements
• Ability to work independently and lead implementation projects with minimal oversight