GMP QA Assistant – Pharma, Day Shift (Maastricht)

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

Vantaggi offerti da questo lavoro

Travel allowance

Pension accrual

Temporary contract via Manpower

Descrizione del lavoro

Manpower is seeking a QA Assistant for a pharmaceutical production environment near Maastricht. This full-time role focuses on ensuring GMP-compliant documentation, batch records, and label processes, with substantial shop-floor exposure.

You will work closely with production, warehouse, and quality teams to ensure accurate documentation and QA reviews, contributing to high-quality manufacturing operations in a highly regulated GMP setting.

Competenze

• No minimum education required.
• English language proficiency required.

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

English

Descrizione del lavoro

Manpower is seeking a QA Assistant for a pharmaceutical production environment near Maastricht. This full-time role focuses on ensuring GMP-compliant documentation, batch records, and label processes, with substantial shop-floor exposure.

You will work closely with production, warehouse, and quality teams to ensure accurate documentation and QA reviews, contributing to high-quality manufacturing operations in a highly regulated GMP setting.