Full-time
Contract QA-IT / CSV Consultant (GxP / GCP)
Posted by Warman O'Brien • , , Spain, , , Spain, Spain
About the Role
We are supporting a leading CRO / consultancy in their search for an experienced QA-IT / Computer System Validation (CSV) Consultant to support GxP and GCP-regulated systems within a clinical environment.
This is a contract role suited to someone confident operating independently and partnering closely with Process and System Owners to ensure compliance, data integrity, and high-quality validation outcomes.
Key Responsibilities
- Support the Process and System Owner in the planning and execution of CSV activities in line with GxP / GCP requirements
- Create, review, and maintain full validation documentation , including:
- Validation Plans
- User Requirements Specifications (URS)
- Validation Reports
- Ensure traceability, consistency, and audit readiness across all validation documentation
- Support compliance with data integrity principles throughout system lifecyc...
Ready to Apply?
Submit your application today and take the next step in your career journey with Warman O'Brien.
Apply Now