QA/QC Officer: GMP Batch Release & Quality Investigator

Air Liquide; Antwerpen; On-site; EUR 42,000 - 65,000; Full time

Job summary

Air Liquide Medical Ltd. NV is hiring a QA/QC Officer to join the Benelux Pharmaceutical / Quality Department in Schelle.

You will support daily GMP/GDP/GMP-related activities and handle batch release for non-medicinal products, ensuring compliance across production and lab areas. Responsibilities include reviewing batch documentation, deviations investigations (OOS), CAPAs, validations, and writing procedures, with strong collaboration across Operations, QA, HSE and suppliers.

Qualifications

• Bachelor’s or Master’s degree in Life Sciences, Bio-engineering, Industrial Pharmacy, Chemistry, or related discipline.
• 0 to 3 years of QA/QC experience in pharmaceutical, biotech, or medical devices; internships valued.

Responsibilities

• Quality Control, Batch Review & Non-Medicinal Release per SOPs and CoA.
• Lead Deviations, OOS investigations and CAPAs with QC Manager oversight.
• validations, qualification activities for equipment and processes.
• Write and update procedures, participate in audits and inspections.

Skills

GMP/GDP/GLP knowledge

Quality investigations

Root-cause analysis

Documentation review

MS Office / Google Workspace

Education

Bachelor’s or Master’s in Life Sciences/related

Tools

MS Office

Google Workspace

Job description

Air Liquide Medical Ltd. NV is hiring a QA/QC Officer to join the Benelux Pharmaceutical / Quality Department in Schelle.

You will support daily GMP/GDP/GMP-related activities and handle batch release for non-medicinal products, ensuring compliance across production and lab areas. Responsibilities include reviewing batch documentation, deviations investigations (OOS), CAPAs, validations, and writing procedures, with strong collaboration across Operations, QA, HSE and suppliers.