Job Description
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.
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.
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