QA/QC Specialist – GMP Compliance & Batch Release

Air Liquide; Schelle; On-site; EUR 52,000 - 75,000; Full time

Job summary

Air Liquide Medical Ltd. NV and Air Liquide Healthcare Netherlands seek a QA/QC Officer to join the Benelux Pharmaceutical/Quality Department at our Schelle GMP site.

You will support daily quality tasks across starting materials to finished products, ensuring GMP, GDP, and MDR/ISO 13485 compliance, and you will be responsible for final batch release of non-medicinal products. You will collaborate with Operations, Production, QA, HSE and external partners, lead investigations, CAPAs, and

Qualifications

• Bachelor’s or Master’s degree in Life Sciences, Bio-engineering, Industrial Pharmacy, Chemistry, or a related scientific discipline.
• 0 to 3 years of experience in a Quality Assurance or Quality Control environment (pharmaceutical, biotech or medical devices).
• First hands-on experience (internship or master thesis) in GMP/GLP environment is valued.

Responsibilities

• Review production and laboratory batch documentation per SOPs and regulatory requirements.
• Perform the final batch release of non-medicinal products and approve CoA sampling at client sites.
• Manage release of raw materials, packaging materials, and intermediate products.
• Lead deviations, OOS investigations and CAPAs related to GMP and quality activities.
• Prepare, execute, and follow up on validation/qualification activities for equipment, analytical instruments, and processes.
• Write and update quality documents and procedures.

Skills

GMP, GDP, GLP

Root-cause analysis

Batch record review

Quality investigations

MS Office/Google Workspace

Education

Bachelor’s or Master in Life Sciences/related field

Job description

Air Liquide Medical Ltd. NV and Air Liquide Healthcare Netherlands seek a QA/QC Officer to join the Benelux Pharmaceutical/Quality Department at our Schelle GMP site.

You will support daily quality tasks across starting materials to finished products, ensuring GMP, GDP, and MDR/ISO 13485 compliance, and you will be responsible for final batch release of non-medicinal products. You will collaborate with Operations, Production, QA, HSE and external partners, lead investigations, CAPAs, and