Senior Qualified Person & Quality Lead (Pharma)

VitalAire Canada Inc.; Belgique; À distance; EUR 110 000 - 140 000; Plein temps

Résumé du poste

Air Liquide is seeking a Quality Control Manager (Qualified Person) for its Schelle facility in Belgium. You will act as the QP for on-site batch release of medicinal products and remotely for cryogenic gas fillings at additional Belgian sites, ensuring GMP compliance and regulatory adherence.

You will lead a 7-person team, drive validation projects, and oversee deviation handling, OOS investigations, and continuous improvement across the Belux region.

Qualifications

• Master's degree in Pharmacy / Pharmaceutical Sciences is required and QP number is required.
• Proven experience in batch release, method validation, process validation, and instrument qualification.
• Strong expertise in GMP, GLP, deviation management, and root-cause analysis (OOS/CAPA).
• Demonstrated track record leading site project initiatives and implementing new products and analytical methods.

Responsabilités

• Act as the Qualified Person (QP) for the Schelle site, ensuring regulatory compliance and batch release of medicinal products.
• Oversee remote QP activities for filling road tankers with cryogenic medicinal gases across two additional Belgian sites.
• Lead a team of 7 and manage daily release activities, deviations, OOS investigations, CAPAs, and quality complaints.

Connaissances

Batch release

Method validation

Process validation

Instrument qualification

GMP knowledge

GLP knowledge

Deviation management

Root cause analysis

Project leadership

Stakeholder management

Formation

Master's degree in Pharmacy / Pharmaceutical Sciences

QP number

Description du poste

Air Liquide is seeking a Quality Control Manager (Qualified Person) for its Schelle facility in Belgium. You will act as the QP for on-site batch release of medicinal products and remotely for cryogenic gas fillings at additional Belgian sites, ensuring GMP compliance and regulatory adherence.

You will lead a 7-person team, drive validation projects, and oversee deviation handling, OOS investigations, and continuous improvement across the Belux region.