Description

You lead validation efforts and ensure requirements traceability across the LabWare LIMS 8 implementation.

This role is on-site.

Responsibilities

• Support validation strategy and execution, including IQ, OQ, and PQ.
• Review validation documentation for completeness and accuracy.
• Collaborate with configuration and integration teams to validate workflows and system functionality.
• Ensure compliance with GxP, CSV, and internal procedures to maintain audit readiness.
• Assist in preparing for regulatory inspections and review validation reports and deviations.

Required Skills

• 10+ years of experience in laboratory or quality environments.
• Proven experience supporting validation of LabWare LIMS, preferably LabWare 8.
• Strong knowledge of CSV, GxP, and GAMP 5 frameworks.
• Experience working in GMP laboratory environments.
• Demonstrated ability to ensure traceability between requirements and system configuration.
• Experience supporting regulatory inspections and audit activities.

Key Skills

Education

Any Graduate