CSV Validation Engineer – Contract

About the role

No deviation is seeking a CSV Validation Engineer on a contract basis to support computer system validation activities for DeltaV automation systems. You will develop and review validation protocols, ensure regulatory compliance, and contribute to the delivery of patient‑centric pharmaceutical solutions.

Key responsibilities

• Develop, review and maintain CSV protocols (IQ, OQ, PQ) for DeltaV systems.
• Support configuration, coding and validation of DeltaV automation platforms.
• Ensure compliance with GAMP 5 and relevant regulatory guidelines throughout the validation lifecycle.
• Perform risk assessments and system impact analyses.
• Review system design specifications and functional documents.
• Coordinate testing activities, resolve validation issues and maintain audit‑ready documentation.

Required profile

• Degree in Engineering, IT or a related discipline.
• Experience with DeltaV systems, preferably with coding or configuration exposure.
• Knowledge of the CSV lifecycle and GAMP 5 guidelines.
• Familiarity with GMP‑regulated environments.
• Strong documentation and review capabilities.
• Effective communication and stakeholder management skills.

Required skills

• DeltaV systems
• CSV lifecycle
• GAMP 5 guidelines
• GMP‑regulated environment

What we offer

• Generous leave policy.
• Comprehensive medical and dental coverage.
• Professional development programs and continuous learning resources.
• Inclusive culture that values innovation, collaboration and diverse perspectives.
• Opportunity to make a tangible impact on the pharmaceutical industry.