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Find your next Digital & IT role in Life Sciences and help drive innovation, data, and system excellence across Belgium’s leading companies.
Our client, a leading pharmaceutical company, is seeking a Cleaning Validation Engineer to specialize in the development and optimization of cleaning processes for production equipment. The role combines technical expertise with operational support to ensure compliance and business continuity within a regulated manufacturing environment.
Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een analytische professional voor een rol gericht op cleaning validatie. De focus van deze functie ligt op het uitvoeren van chromatografische analyses en het waarborgen van kwaliteitsstandaarden binnen een gereguleerde omgeving.
Our client, a global life sciences organization, is seeking a Quality Performance Lead to play a pivotal role within a major quality management system transformation. This role focuses on the end-to-end design and implementation of a quality performance framework and KPI pyramid to drive data-driven decision-making.
Our client, a leading life sciences organization, is seeking a Project Validation Coordinator for an intensive graduate program. This role focuses on coordinating validation deliverables and project scheduling to ensure the successful execution of high-quality technical projects.
Our client, a leading pharmaceutical manufacturing organization, is seeking a process owner for their site-wide quality systems. This role focuses on driving compliance and continuous improvement for validation processes while serving as a subject matter expert during regulatory inspections.
Our client, a leading pharmaceutical company, is looking for a Commissioning Lead to drive the execution of an ambitious project. This role involves overseeing the entire commissioning lifecycle, bridging the gap between engineering, contractors, and quality departments to ensure successful delivery of critical installations.
Notre client, une organisation de premier plan dans le secteur des sciences de la vie, recherche un profil expérimenté pour superviser les activités de contrôle qualité sur son site. Ce rôle consiste à garantir la libération des produits finis et des matières premières tout en assurant la conformité aux normes de qualité les plus strictes. Le projet implique la gestion d'une équipe technique et le pilotage de l'amélioration continue des systèmes de qualité.
For the start-up of a new production facility we are looking for a Change control coordinator/Quality operational readiness officer. This critical role serves as the Change Control Coordinator while providing technical quality oversight for facility construction, modifications and utility upgrades. The position ensures seamless transition from construction phases to operational status while maintaining full GMP compliance throughout the transformation process.
Design, implement, and validate digital systems that support GMP manufacturing, ensure data integrity, and enable efficient, compliant operations across life sciences environments.
MES Consultant – Implement and optimize MES to support efficient, compliant manufacturing.
CSV Consultant – Validate GxP systems and ensure regulatory-compliant digital solutions.
MES Specialist – Configure and maintain MES to support production operations.
MBR Editor – Create and update accurate electronic batch records.
MBR Designer – Design structured, compliant electronic batch workflows.
MBR Reviewer – Review and approve electronic batch records for accuracy.
Master Batch Editor – Maintain and update Master Batch documentation.
Master Batch Reviewer – Ensure GMP-compliant batch record quality.
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