Senior Qualified Person & Quality Leader — GMP

Air Liquide; Belgique; Presencial; EUR 90.000 - 130.000; Jornada completa

Descripción de la vacante

Air Liquide Medical SA in Belgium is seeking a Quality Manager & Qualified Person to oversee on-site and remote QP activities for multiple Belgian sites. You will ensure GMP-compliant batch release, lead a small quality team, and drive validation projects and continuous improvement across the facility.

The role requires a Master’s degree in Pharmacy / Pharmaceutical Sciences (QP) and 8–10 years’ experience as a QP, with strong GMP/GLP expertise and leadership skills.

Formación

• Master's degree in Pharmacy / Pharmaceutical Sciences with QP number.
• 8 to 10 years of experience as a Qualified Person (QP) in pharmaceutical manufacturing and QC.
• Strong expertise in GMP, GLP, deviation management, and root-cause analysis (OOS/CAPA).
• Proven leadership and people management skills with an empowering, collaborative approach.

Responsabilidades

• Act as the Qualified Person (QP) for the manufacturing site in Schelle, ensuring full regulatory compliance and timely batch release of medicinal products.
• Act as the Qualified Person (QP) remotely for the filling of road tankers with cryogenic medicinal gases across two additional Belgian sites.
• Oversee quality control activities and certify that each production batch has been manufactured and checked in accordance with GMP and Marketing Authorizations.
• Lead and coach a team of 7 team members and oversee daily operations related to batch release, deviations, OOS investigations, CAPAs and product quality complaints.

Conocimientos

QP responsibilities

Batch release

GMP/GLP

Leadership

Regulatory compliance

Educación

Master's degree in Pharmacy / Pharmaceutical Sciences

Descripción del empleo

Air Liquide Medical SA in Belgium is seeking a Quality Manager & Qualified Person to oversee on-site and remote QP activities for multiple Belgian sites. You will ensure GMP-compliant batch release, lead a small quality team, and drive validation projects and continuous improvement across the facility.

The role requires a Master’s degree in Pharmacy / Pharmaceutical Sciences (QP) and 8–10 years’ experience as a QP, with strong GMP/GLP expertise and leadership skills.