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Quality Engineer (MES & Cleaning Validation)

Belgium, Geel · Job Posted May 27, 2026
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Job Description

Are you ready to make a tangible impact on global health? Join a world-class leader in pharmaceutical innovation at the Centre of Excellence in Geel. As part of the Supply Chain Quality team, you will play a crucial role in the launch, growth, and final release of Synthetic APIs that improve lives worldwide. If you are a quality-minded professional with a strong technical backbone and a passion for operational excellence, this is your opportunity to elevate your career.

Job Responsibility

  • Review and approve Master Batch Records and technical recipes to ensure accurate and compliant commercial API production
  • Perform data extraction, abstract material reviews, and author, review, and approve relevant QA procedures
  • Deliver essential quality oversight for cleaning validation processes
  • Support small-scale optimization projects and daily tasks within the QA Commercial Operations team
  • Act as a strong, communicative partner, fostering collaboration between Business and Quality stakeholders

Requirements

  • Bachelor's degree or higher in life sciences, chemistry, biology, pharmacy, engineering, or information technology
  • Minimum of 3 years of experience in Chemical/Pharmaceutical Supply Chain or Quality Assurance
  • Strong understanding of manufacturing operations, production systems, and GMP environments
  • Experience with cleaning validation is required
  • Proficiency with the PAS-X Manufacturing Execution System (MES) is an asset
  • Familiarity with Delta-V systems is a plus
  • Professional proficiency in English

Nice to have

  • Proficiency with the PAS-X Manufacturing Execution System (MES)
  • Familiarity with Delta-V systems

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