QA Assistant - Uitzendbureau.nl

Jobster; Geleen; On-site; EUR 33,000 - 42,000; Full time

Benefits offered by this job

Travel allowance according to company

Pension accrual through Manpower

Temporary employment contract through

Job summary

Manpower is seeking a QA Assistant for a pharmaceutical production environment near Maastricht. The role focuses on ensuring documentation, batch records, and GMP label processes are completed accurately and in compliance, with substantial time on the shop floor.

You will work with production, warehouse, and quality teams, performing QA reviews, and supporting audits within a highly regulated GMP setting. The assignment runs from 16 November 2026 to 14 March 2027.

Qualifications

• Experience in QA within a GMP-regulated environment.
• Familiar with batch records and GMP label processes.

Responsibilities

• Issuing, controlling, and reconciling GMP labels.
• Verifying label requests against approved docs and schedules.
• Reviewing label issuance records and discrepancies.
• Reviewing batch records and logbooks.
• Approving manufacturing documentation including batch records.
• Identifying and escalating documentation errors and GMP concerns.
• Supporting batch disposition through QA reviews.
• Performing routine shop floor quality oversight.
• Collaborating with Manufacturing, Warehouse and Quality Systems teams.
• Supporting audits and inspections.

Skills

Quality Assurance

GMP compliance

Documentation

Shop floor

Job description

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.