QA/QC Specialist - GMP Batch Release & Quality

Air Liquide; Schelle; On-site; EUR 42,000 - 64,000; Full time

Job summary

Air Liquide is seeking a QA/QC Officer to support the Benelux Pharmaceutical/Quality Department at the Schelle GMP site. You will oversee final batch release of non-medicinal products, review batch documentation, manage material releases, and lead quality investigations to ensure GMP/GDP/ISO13485 compliance across production and lab areas.

The ideal candidate holds a Life Sciences degree, 0–3 years' QA/QC experience in pharma/medical devices, and strong analytical, communication, and

Qualifications

• Bachelor’s or Master’s degree in Life Sciences or related field.
• 0 to 3 years of experience in a Quality Assurance or Quality Control environment (pharmaceutical, biotech, or medical devices).
• First hands-on experience (including internship or master thesis) in a GMP/GLP environment is highly valued.
• Good theoretical knowledge or practical exposure to pharmaceutical guidelines and quality frameworks: GMP, GDP, GLP, Ph. Eur., and ISO 13485 / MDR.
• Proficiency with IT systems (MS Office, Google Workspace).

Responsibilities

• Review production and laboratory batch documentation in accordance with internal SOPs, regulatory requirements, and customer quality agreements.
• Perform the final batch release of non-medicinal products and approve certificates of analysis (CoA) for sampling at client sites.
• Manage the release of raw materials, packaging materials, and intermediate products used in production.
• Conduct regular quality tours and monitor compliance with GMP and flow/zoning in both production and lab areas.
• Lead investigations and draft detailed reports for deviations, OOS results, customer complaints, and non-conformities.

Skills

GMP/GDP/GLP knowledge

Pharmacopoeia/quality standards

Root-cause analysis (OOS/CAPA)

Batch record review

Quality investigations

Education

Bachelor’s or Master’s degree in Life Sciences or related field

Tools

MS Office

Google Workspace

Job description

Air Liquide is seeking a QA/QC Officer to support the Benelux Pharmaceutical/Quality Department at the Schelle GMP site. You will oversee final batch release of non-medicinal products, review batch documentation, manage material releases, and lead quality investigations to ensure GMP/GDP/ISO13485 compliance across production and lab areas.

The ideal candidate holds a Life Sciences degree, 0–3 years' QA/QC experience in pharma/medical devices, and strong analytical, communication, and