Job Description & How to Apply Below
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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