Contract:
Temporary / 5 Month Contract (until March 2027)
Location:
Geleen, Netherlands (Onsite)
Hours:
Full-time (40 hours per week)
Sector:
Quality Assurance / GMP Manufacturing / Life Sciences
About the Role
We are looking for a QA Assistant to join a pharmaceutical manufacturing site in Geleen. This role combines shop floor quality support with GMP documentation review and label management activities. You will work closely with Manufacturing, Warehouse, and Quality teams to ensure compliance, documentation accuracy, and smooth production operations.
The position has been opened as cover for long-term sickness absence and offers hands-on exposure to quality assurance activities within a highly regulated GMP environment.
Key Responsibilities
Issue, control, reconcile, and maintain accountability of GMP labels
Verify label requests against approved documentation and production requirements
Review completed label issuance records and investigate discrepancies
Perform Operational and Aseptic Processing (APS) batch record reviews
Review manufacturing documentation, batch records, logbooks, and supporting records
Identify, document, and escalation GMP documentation errors and compliance issues
Support batch disposition activities through timely QA reviews
Provide routine shop floor QA support and GMP oversight
Collaborate with Manufacturing, Warehouse, and Quality Systems teams
Support audits, inspections, and regulatory compliance activities
Participate in continuous improvement initiatives within Quality Assurance
Who We're Looking For
Experience within Quality Assurance, GMP manufacturing, or another regulated environment
Strong attention to detail and documentation review skills
Understanding of GMP regulations and quality compliance principles
Ability to identify and escalation quality-related issues
Strong communication and stakeholder management skills
Ability to work accurately in a production environment
Proactive and quality-focused mindset
Preferred
Experience with GMP label management and reconciliation
Experience reviewing manufacturing documentation and batch records
Exposure to pharmaceutical or aseptic manufacturing environments
Experience supporting audits and inspections
Knowledge of deviation management and quality investigations
Background in pharmaceutical, biotech, or life sciences manufacturing
Familiarity with batch release and disposition processes
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QA Assistant in Geleen werkgever: Real
Als Production Operator bij ons in Breda maak je deel uit van een dynamisch team dat zich inzet voor de productie van hoogwaardige medicijnen. We bieden een gestructureerde en veilige werkomgeving waar kwaliteit en teamwork centraal staan, met volop mogelijkheden voor persoonlijke groei en ontwikkeling. Met een focus op GMP-normen en een cultuur van continue verbetering, zorgen we ervoor dat onze medewerkers zich gewaardeerd en ondersteund voelen in hun rol.
