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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)