Quality Assurance || Manufacturing Systems / Facility & Utility
&##Support 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.
Review 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.
Communicate quality and compliance status to QA stakeholders.
Experience in pharmaceutical or chemical industry qualification activities.
Experience with manufacturing and/or facility & utility systems.
Fluent in English and Dutch.
Full-time