Ingénieur validation CSV - Belgium - Freelance

Context

We seek an experienced Validation Engineer specializing in Computer System Validation (CSV) for GxP-regulated pharmaceutical environments.

You will validate computerized systems throughout their lifecycle—from system categorization and user requirements to system impact analysis and validation testing (IQ, OQ, PQ)—ensuring compliance with Sanofi standards and regulatory requirements.

Missions

• Author and maintain comprehensive validation documentation
• Execute CSV activities for DCS and PLC automated systems, including interfaces (Design Qualifications, System Impact Analysis, IQ/OQ/PQ Protocols, Testing, Reports)
• Ensure GxP regulatory compliance across all validated systems
• Support change control processes and deviation management

Tools & Environment

• Automated systems such as Emerson DeltaV, Siemens PLC/HMI (preferred)
• Validation documentation and protocols (IQ, OQ, PQ)
• Regulatory frameworks: 21 CFR Part 11, EU Annex 11, GAMP 5
• Platforms: Kneat (preferred)
• IT infrastructure qualification (plus)

Working Conditions

• Validation role within a GxP-regulated pharmaceutical environment
• Collaboration with System Owners, Engineering, and CQV teams
• Focus on audit-ready deliverables and regulatory compliance
• Emphasis on risk-based validation approach and multidisciplinary project coordination