GMP QA Assistant – Pharma (Maastricht Area), 40h

Jobster; Geleen; In loco; EUR 33.000 - 42.000; Tempo pieno

Vantaggi offerti da questo lavoro

Travel allowance

Temporary contract via Manpower

Pension accrual via Manpower

Descrizione del lavoro

Jobster is seeking a QA Assistant for a pharmaceutical production environment near Maastricht. The role focuses on ensuring documentation, batch records, and GMP label processes meet quality standards, with significant shop floor involvement.

You will collaborate with Production, Warehouse, and Quality teams, support audits and inspections, and ensure compliant labeling and documentation. The assignment runs from 16 November 2026 to 14 March 2027, offering a full-time 40-hour schedule and a

Competenze

• Experience in a GMP-regulated pharmaceutical environment.
• Familiar with batch records, labels, and QA review.
• Able to work on the shop floor across production and warehouse.
• Full-time role, 40 hours per week.

Mansioni

• 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.

Conoscenze

GMP knowledge

Quality assurance

Documentation control

Shop floor experience

Descrizione del lavoro

Jobster is seeking a QA Assistant for a pharmaceutical production environment near Maastricht. The role focuses on ensuring documentation, batch records, and GMP label processes meet quality standards, with significant shop floor involvement.

You will collaborate with Production, Warehouse, and Quality teams, support audits and inspections, and ensure compliant labeling and documentation. The assignment runs from 16 November 2026 to 14 March 2027, offering a full-time 40-hour schedule and a