Quality Assurance || Manufacturing Systems / Facility & Utility
Geel, Belgium – Onsite
Role Overview
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.
Responsibilities
* 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.
* Follow up on deviations during qualification activities.
* Communicate quality and compliance status to QA stakeholders.
Key Requirements
* Experience 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.
Practicalities
* Geel, Belgium
* Full-time
* Onsite
Interested? Apply now or send your CV to l.ormrod@panda-int.com