Clinical QMS Lead for EU GMP

Pauwels Consulting in Belgium is seeking a senior quality management expert to assess and enhance a QMS in alignment with EU GMP requirements for clinical trial manufacturing and importation.You will drive remediation priorities, lead the Manufacturing Import Authorization project, and support Health Authority inspections by ensuring readiness of CAPA,...

This role as quality specialist – Clinical QP needs to assess and strengthen the Quality Management System in alignment with applicable EU GMP requirements. The function supports inspection readiness and the Manufacturing Import Authorization project by identifying gaps, defining actins, and enabling compliant processes for clinical product...

Mission Overview: We are seeking a Quality Specialist – Clinical QP for a consultancy mission at a client site, representing Keystone Solutions. In this role, you will assess and strengthen the Quality Management System (QMS) in alignment with applicable EU GMP requirements, supporting inspection readiness and the Manufacturing Import Authorization...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to...

EngiFlex in Belgium is seeking a Quality Specialist - Clinical QP to strengthen the quality management system and support the MIA project for clinical products.You will lead gap assessments, define corrective actions, and ensure inspection readiness across document control, deviations, CAPA, and release processes. The role requires deep EU GMP knowledge and...

Tasks and responsibilities As Quality Specialist - Clinical QP, you will evaluate and reinforce the quality management system in line with applicable EU GMP requirements. The role contributes to inspection readiness and supports the Manufacturing Import Authorization project by identifying gaps, defining corrective actions, and enabling compliant processes...

We’re hiring: Head of GMP Unit – ATMP | Ghent University Hospital (Belgium) CellGENTherapies, part of the Department of Human Bodily Materials at Ghent University Hospital, is entering an exciting new phase. A brand-new GMP facility, currently under construction and operational in 2027, will significantly expand our capacity to develop and manufacture...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

Our client, a leading life sciences organization, is seeking a specialist to assess and enhance a quality management system in alignment with EU GMP requirements. The role supports inspection readiness and a manufacturing import authorization project to enable compliant processes for clinical product certification. Responsibilities Review and assess the...