CSV - Validation Lead

We are currently looking for an experienced GxP Validation Consultant to support a regulated environment on a critical programme of work for a Global Pharmaceutical client.

Project length - 5 Months + Possible extension

Location - Remote

Start date - Mid February

Industry - Pharmaceutical

CSV / Validation Lead

Role Summary:

Ensures the project meets GxP , 21 CFR Part 11 , and global serialization validation requirements.

Key Responsibilities:

• Create GxP validation plan and validation approach
• Develop IQ/OQ/PQ, RTM, protocols, SOP updates
• Support testing teams in executing validation scripts
• Ensure audit‑ready documentation for regulatory agencies
• Manage deviation and CAPA processes

Required Skills:

• Deep GxP/CSV knowledge
• Experience validating SAP ATTP, ERP, MES
• Strong documentation and audit preparation experience

If you are available and interested, or would like more details, please get in touch.