Quality Assurance || Manufacturing Systems / Facility & Utility📍 Geel, Belgium – OnsiteRole OverviewSupport the QA Engineering department in ensuring that all qualification-related regulatory and procedural requirements are met throughout the full lifecycle (concept to retirement) of manufacturing, facility, and utility systems within a pharmaceutical environment. The role ensures ongoing cGMP compliance and quality oversight during projects and operations.ResponsibilitiesReview and approve qualification documentation (SOPs, URS, risk assessments, test plans, change controls, deviations, CAPAs).Ensure compliance with cGMP regulations and internal quality standards.Provide QA support for new and upgraded systems.Participate in cross-functional engineering project teams.Follow up on deviations during qualification activities.Communicate quality and compliance status to QA stakeholders.Key RequirementsExperience in pharmaceutical or chemical industry qualification activities.Knowledge of cGMP regulations.Experience with manufacturing and/or facility & utility systems.Familiar with change management and document systems (e.G., Trackwise, TruVault, Kneat).Strong communication skills.Fluent in English and Dutch.PracticalitiesGeel, BelgiumFull-timeOnsite Interested? Apply now or send your CV to l.ormrod@panda-int.com