QA/QC Specialist — GMP & MDR Compliance (Belgium)

VitalAire Canada Inc.; Schelle; Remote; EUR 45,000 - 70,000; Full time

Job summary

Air Liquide Medical Ltd. NV in Schelle, Belgium, is seeking a QA/QC Officer to support the Benelux Pharmaceutical / Quality Department, reporting to the Quality Control Manager.

You will perform batch release, review documentation, and ensure GMP, GDP, and MDR/ISO 13485 compliance across medicinal and non-medicinal products. This role collaborates with Operations, QA, HSE, Maintenance, and external partners, conducts deviations and investigations, and contributes to audits and PQR writing, while

Qualifications

• Strong understanding of GMP, GDP, GLP and ISO 13485/MDR frameworks.
• Experience with batch release and certificate of analysis approvals.
• Familiarity with quality investigations and CAPA processes.

Responsibilities

• Review production and laboratory batch documentation.
• Perform final batch release of non-medicinal products and approve COAs.
• Lead deviations and OOS investigations and report findings to QC manager.
• Coordinate Change Controls and CAPAs related to GMP activities.
• Prepare and update SOPs, PQs, and PQRs; support audits and inspections.

Skills

Quality investigations

Batch review

GMP knowledge

Analytical thinking

Communication

Education

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

Tools

MS Office

Laboratory information systems

Job description

Air Liquide Medical Ltd. NV in Schelle, Belgium, is seeking a QA/QC Officer to support the Benelux Pharmaceutical / Quality Department, reporting to the Quality Control Manager.

You will perform batch release, review documentation, and ensure GMP, GDP, and MDR/ISO 13485 compliance across medicinal and non-medicinal products. This role collaborates with Operations, QA, HSE, Maintenance, and external partners, conducts deviations and investigations, and contributes to audits and PQR writing, while