Full-time

Contract QA-IT / CSV Consultant (GxP / GCP)

Posted by Warman O'Brien • , , Spain, , , Spain, Spain

📍 , , Spain, , , Spain 🕒 February 22, 2026

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