QA Assistant in Geleen

Vacaturebeschrijving

Do you have experience within Quality Assurance and enjoy working in a GMP-regulated environment where accuracy truly matters? Are you looking for a full-time position with a competitive salary, valuable experience in the pharmaceutical industry, and the opportunity to play an important role in maintaining quality standards? Then this QA Assistant position could be the next step in your career.

Employment agency Manpower is looking for a QA Assistant for a pharmaceutical production environment near Maastricht.

As a QA Assistant, you will support manufacturing operations by ensuring that documentation, batch records, and GMP label processes are completed correctly and in compliance with quality requirements. You will work closely with production, warehouse, and quality teams and spend a significant part of your time on the shop floor.

Your responsibilities

• Issuing, controlling, and reconciling GMP labels
• Verifying label requests against approved documentation and production schedules
• Reviewing label issuance records and investigating discrepancies
• Reviewing operational and aseptic processing batch records
• Approving manufacturing documentation, including batch records and logbooks
• Identifying and escalating documentation errors, deviations, and GMP concerns
• Supporting batch disposition activities through timely QA reviews
• Performing routine shop floor quality oversight activities
• Collaborating with Manufacturing, Warehouse, and Quality Systems teams
• Supporting audits, inspections, and compliance-related activities

What's in it for you?

• Gross monthly salary between €3,000 and €3,800
• Full-time position of 40 hours per week
• Travel allowance according to company policy
• Temporary employment contract through Manpower
• Pension accrual through Manpower
• Opportunity to gain experience within a highly regulated GMP environment
• Valuable exposure to pharmaceutical manufacturing processes
• Assignment running from 16 November 2026 until 14 March 2027
• Professional and quality-focused working environment

Over de werkgever

You will be joining an international organization within the pharmaceutical and life sciences sector. The site operates in a highly regulated GMP environment where quality, compliance, patient safety, and accurate documentation are central to daily operations. Together with colleagues from production, warehousing, and quality departments, you will contribute to maintaining high quality standards and supporting critical manufacturing processes.

Working hours
This is a full-time position in day shift.