QA/QC Specialist: GMP Compliance & Batch Release

BE10805-ALBENEL Air Liquide Medical SA; Schelle; On-site; EUR 52,000 - 68,000; Full time

Job summary

Air Liquide Medical Ltd. NV is seeking a QA/QC Officer in Schelle to support GMP/GDP compliance and batch release for medicinal and non-medicinal products.

You will work closely with Operations, Production, QA, HSE and external partners to ensure strict quality standards across the manufacturing chain. The role involves deviations, OOS investigations, CAPAs, validation/qualification activities, and contribution to PQR and audit preparations, with a focus on continuous improvement and regulatory

Qualifications

• Bachelor’s or Master’s degree in Life Sciences or related field.
• 0 to 3 years of experience in QA/Quality Control (pharmaceutical, biotech or medical devices).
• GMP/GLP experience valued, with hands-on exposure during internships or theses.

Responsibilities

• Quality Control, Batch Review & Non-Medicinal Release Review of production and lab documentation.
• Perform final batch release of non-medicinal products and CoA approvals.
• Manage release of raw materials, packaging materials and intermediates.
• Conduct regular quality tours and monitor GMP compliance in production and lab areas.
• Lead investigations for deviations, OOS results and CAPAs.
• Prepare and follow up on validation and qualification activities for equipment and processes.
• Write and update SOPs and related quality documents; produce PQRs.
• Support site inspections and audits across sites.
• Deliver GMP, GDP and pharmacovigilance training to QC and production staff.

Skills

Quality Control

Quality Assurance

GMP

GDP

GLP

Root cause analysis

Documentations

Audits

Education

Bachelor’s or Master’s degree in Life Sciences, Bio-engineering, Industrial Pharmacy, Chemistry

Tools

MS Office

Google Workspace

Job description

Air Liquide Medical Ltd. NV is seeking a QA/QC Officer in Schelle to support GMP/GDP compliance and batch release for medicinal and non-medicinal products.

You will work closely with Operations, Production, QA, HSE and external partners to ensure strict quality standards across the manufacturing chain. The role involves deviations, OOS investigations, CAPAs, validation/qualification activities, and contribution to PQR and audit preparations, with a focus on continuous improvement and regulatory