GMP QA Assistant - On-Site, Full-Time Pharma

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

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.