Quality Assurance Lead

Responsibilities

• Maintain the Quality Management System according to GDP (medicines) and ISO 13485/MDR (medical devices) standards.
• Lead key quality processes including document management, complaint and CAPA management, and management of change.
• Perform internal auditing and prepare for external audits and inspections.
• Manage supplier qualification and evaluation processes.
• Oversee inventory integrity by monitoring storage conditions, expiry dates (FEFO), and pest control protocols.
• Raise quality awareness among personnel and participate in training and qualification processes.
• Collaborate with the Benelux Quality & Safety Manager to harmonize quality processes between Belgium and the Netherlands.

Requirements

• Master in Science or equivalent degree.
• 3-5 years of professional experience, including experience in a quality environment related to medical devices and/or medicines.
• Fluency in both Dutch and English (written and spoken).
• Strong transversal leadership, analytical skills, and the ability to influence others positively.
• Pragmatic, organized, and able to set priorities in a fast-paced environment.

Preferred Qualifications

• Proficiency in French is a significant plus.

About the Company

Air Liquide is a world leader in gases, technologies, and services for Industry and Health. We leverage energy and environmental transitions, healthcare changes, and digitization to deliver value to our stakeholders through an open, collaborative, and respectful environment.