Computer System Validation Engineer

Computer System Validation Engineer (CSV Engineer)

Location: Verviers, Belgium (on-site)

Languages: Fluent in French and English

Duration: 6-month contract

Our client, a leading organisation in the life sciences sector, is looking for a talented Computer System Validation Engineer (CSV Engineer) to join their team in Verviers. This is a fantastic opportunity to play a key role in ensuring compliance, quality, and data integrity across critical systems within an innovative and collaborative environment.

About the Role

As a CSV Engineer, you’ll oversee the full validation lifecycle for manufacturing, laboratory, and business systems, ensuring they meet GxP regulations and company procedures. You’ll collaborate with project teams, system owners, and vendors to deliver compliant and reliable systems that support product quality and patient safety.

Key Responsibilities

• Manage end-to-end validation of computerized systems
• Prepare and execute validation documentation (URS, IQ/OQ/PQ protocols, traceability matrices, reports)
• Conduct risk assessments and periodic reviews to ensure systems remain compliant
• Work with vendors and internal teams to support system implementation and upgrades
• Maintain complete and traceable CSV documentation
• Support training and provide user guidance for validated systems

About You

• Degree (or equivalent experience) in Life Sciences or a related field
• Experience in Computer System Validation within a GxP-regulated environment
• Strong knowledge of data integrity and validation principles
• Excellent written and verbal communication in French and English
• Detail-oriented, organised, and proactive with a strong team spirit

If you are interested in finding out more about this role or others, please contact Jada Kirlew at jkirlew@i-pharmconsulting.com or call: +44 (0)20 7551 0727