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Ingénieur validation CSV - Belgium

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Hybrid

Ingénieur validation CSV - Belgium

Salutech

Ingénieur validation CSV - Belgium

Skills

Computer System Validation (CSV)GxPGMPData Integrity21 CFR Part 11GAMP 5

2 days ago

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Important information


Contract type:

Freelance / Contract

Daily rate:

Salary according to profile

Location:

2440 Geel, Belgium

Work mode:

Hybrid

Published on:

1 October 2026

What they need


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

Profile wanted


  1. 2-3 years validation experience with CSV exposure
  2. Strong knowledge of change control and deviation management
  3. Expertise in GMP guidelines and Data Integrity principles
  4. Regulatory compliance knowledge: 21 CFR Part 11, EU Annex 11, GAMP 5
  5. Hands-on automated systems validation experience
  6. Experience with process automation systems (Emerson DeltaV, Siemens PLC/HMI) (preferred)
  7. Design Qualification execution experience (preferred)
  8. Familiarity with risk-based validation approach (preferred)
  9. Knowledge of upstream/downstream bioprocessing (preferred)
  10. Experience in Sanofi environment (preferred)
  11. Experience with Kneat platform (preferred)
  12. IT infrastructure Qualification (plus)
  13. Analytical mindset with systematic problem-solving abilities
  14. Structured approach to multidisciplinary project coordination
  15. Strong documentation skills for audit-ready deliverables
  16. Proactive compliance awareness with risk identification capabilities
  17. Excellent communication for cross-functional collaboration with System Owners, Engineering, and CQV teams

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