QA/QC Batch Release Specialist – GMP, GDP & MDR

Air Liquide Healthcare; Schelle; On-site; EUR 45,000 - 65,000; Full time

Job summary

Air Liquide Healthcare Belgium is seeking a QA/QC Officer to support the Benelux Pharmaceutical/Quality Department at the Schelle GMP site. You will monitor quality tasks from starting materials to finished products and ensure strict GMP/GDP compliance with MDR/ISO 13485 requirements.

You will collaborate with Operations, Production, QA, HSE, Maintenance, Engineering, and external suppliers, participating in deviations, OOS investigations, qualifications/validation, PQR, and audit preparations.

Qualifications

• Bachelor’s or Master’s degree in Life Sciences or related field.
• 0–3 years of experience in QA/QC in pharma/medical devices; GMP/GLP exp valued.
• Knowledge of GMP, GDP, ISO13485 and MDR.

Responsibilities

• Review batch documentation according to SOPs, regulations and quality agreements.
• Perform final release of non-medicinal products and approve COA for sampling at client sites.
• Release of raw materials, packaging materials and intermediates used in production.
• Lead investigations for deviations/OOS and prepare CAPAs.

Skills

GMP & GDP

Root-cause analysis

Batch review

CAPA/Deviations

Quality investigations

IT systems

Education

Bachelor/Master in Life Sciences

Tools

MS Office

Google Workspace

Job description

Air Liquide Healthcare Belgium is seeking a QA/QC Officer to support the Benelux Pharmaceutical/Quality Department at the Schelle GMP site. You will monitor quality tasks from starting materials to finished products and ensure strict GMP/GDP compliance with MDR/ISO 13485 requirements.

You will collaborate with Operations, Production, QA, HSE, Maintenance, Engineering, and external suppliers, participating in deviations, OOS investigations, qualifications/validation, PQR, and audit preparations.