QA/QC Officer

Main tasks

Quality Control, Batch Review & Non-Medicinal Release

• 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.

Deviations, OOS & Quality Investigations

• Lead investigations and draft detailed reports for deviations, Out of Specification (OOS) results, customer complaints, and non-conformities, reporting findings directly to the QC Manager.
• Handle Change Controls and CAPAs (Corrective and Preventive Actions) related to GMP and quality activities.

Validations, Projects & Continuous Improvement

• Prepare, execute, and follow up on validation and qualification activities for equipment, analytical instruments, and processes in production and laboratory areas.
• Author and update written procedures, manuals, SOPs, and related quality documents.
• Write the annual Product Quality Review (PQR) for medicinal products.
• Support the preparation and execution of site health authority inspections, customer audits, supplier audits, and internal self-inspections across sites.

Training & Compliance

• Deliver GMP, GDP, and Pharmacovigilance training to QC operators, production personnel, warehouse staff, and drivers.
• Ensure continuous compliance with local and European pharmaceutical regulations, Ph. Eur., and medical device standards.

Are you a MATCH?

Profile

Education & Experience

• 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 (including internship or master thesis) in a GMP/GLP environment is highly valued.

Technical & Quality Skills

• Good theoretical knowledge or practical exposure to pharmaceutical guidelines and quality frameworks: GMP, GDP, GLP, Ph. Eur., and ISO 13485 / MDR.
• Strong interest in quality investigations, root-cause analysis (OOS/CAPA), batch record review, and compliance.
• Basic understanding or first exposure to equipment/process validation and qualification activities.
• Proficiency with IT systems (MS Office, Google Workspace).

Personal & Interpersonal Skills

• Highly structured, rigorous, and attentive to detail with a strong quality mindset.
• Eager to learn, proactive, and open to feedback, with the motivation to grow within a pharmaceutical operational environment.
• Excellent communication and interpersonal skills to collaborate smoothly with multidisciplinary teams (Production, Maintenance, HSE, Affiliates).
• Pragmatic problem-solver who stays calm, composed, and efficient under pressure or during unexpected situations.

Languages

• Fluent in Dutch and English (written and spoken).
• Knowledge of French is a strong asset (nice to have)

Our Differences make our Performance

At Air Liquide, we are committed to build a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.

We welcome and consider applications from all qualified applicants, regardless of their background. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world.