QA/QC Officer

Air Liquide Healthcare; Schelle; On-site; EUR 45,000 - 65,000; Full time

Job summary

Air Liquide Healthcare Belgium is seeking a QA/QC Officer to support the Benelux Pharmaceutical/Quality Department at the Schelle GMP site. You will monitor quality tasks from starting materials to finished products and ensure strict GMP/GDP compliance with MDR/ISO 13485 requirements.

You will collaborate with Operations, Production, QA, HSE, Maintenance, Engineering, and external suppliers, participating in deviations, OOS investigations, qualifications/validation, PQR, and audit preparations.

Qualifications

• Bachelor’s or Master’s degree in Life Sciences or related field.
• 0–3 years of experience in QA/QC in pharma/medical devices; GMP/GLP exp valued.
• Knowledge of GMP, GDP, ISO13485 and MDR.

Responsibilities

• Review batch documentation according to SOPs, regulations and quality agreements.
• Perform final release of non-medicinal products and approve COA for sampling at client sites.
• Release of raw materials, packaging materials and intermediates used in production.
• Lead investigations for deviations/OOS and prepare CAPAs.

Skills

GMP & GDP

Root-cause analysis

Batch review

CAPA/Deviations

Quality investigations

IT systems

Education

Bachelor/Master in Life Sciences

Tools

MS Office

Google Workspace

Job description

Air Liquide Medical Ltd. NV and Air Liquide Healthcare Netherlands provide healthcare professionals and patients with solutions that contribute to our mission of protecting vulnerable lives. We are constantly inventing and developing solutions for healthcare facilities. In the Hospital Care (Belux) business, our employees serve more than 7,500 hospitals and clinics every day, supplying them with oxygen and other medical gases. In the Homecare business (Belux), our employees take care of the respiratory treatment at home of, among others, more than 40,000 patients.

How will you CONTRIBUTE and GROW?

As QA/QC Officer, you are part of the Benelux Pharmaceutical / Quality Department and you report directly to the Quality Control Manager (Qualified Person).

In this role, you work closely with the QC Manager to provide daily operational support for all pharmaceutical and quality tasks related to the production of medicinal and non-medicinal products at our European GMP site in Schelle. As a key quality support, you monitor quality tasks for the entire chain, from starting materials to finished products, while ensuring strict compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and Medical Device requirements (MDR, ISO 13485). You are also directly responsible for the final batch release of non-medicinal products and raw materials.

You collaborate closely with various internal stakeholders (Operations, Production, QA, HSE, Maintenance, Engineering, Sales) as well as external affiliates and suppliers, actively participating in deviations, Out of Specification (OOS) investigations, qualification/validation activities, Product Quality Reviews (PQR), and audit preparations.

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.