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Trouvez votre prochain poste en Digital & IT dans les Life Sciences et contribuez à stimuler l’innovation, la gestion des données et l’excellence des systèmes au sein des principales entreprises de Belgique.
Onze klant, een internationale speler in de farmaceutische sector, is op zoek naar een gedreven CSV Engineer om hun kwaliteit en- validatie team te versterken. Je komt terecht in een dynamische werkomgeving waar je de volledige verantwoordelijkheid draagt voor de validatiestatus van IT-systemen binnen een gereguleerde productieomgeving.
Our client, a leading player in the field of occupational health and wellbeing, is seeking an Associate Medical Manager to strengthen its operations in the Brussels region. In this hybrid role, you will combine your practical medical expertise with a role providing strategic support and coaching to a team of passionate doctors, within an organisation that values a healthy work-life balance.
Our client, a leading life sciences organization, is seeking an expert to lead comprehensive regulatory dossier assessments and file gap analyses. The project focuses on identifying compliance risks and developing scientific justifications to support regulatory submissions and health authority responses.
Our client, a leading biopharmaceutical organization, is seeking an expert to drive analytical excellence within their manufacturing science and technology department. This role focuses on developing and implementing critical analytical methods to ensure the quality and consistency of cell culture-based production processes across an international biologics network.
Our client is seeking a Compliance Engineer to serve as the primary point of contact for quality and compliance matters within their technical operations. This role bridges the gap between engineering, maintenance, and qualification by ensuring all processes align with rigorous quality standards.
Our client, a global pharmaceutical organization, is seeking a professional to oversee the quality management of third-party computerized systems providers. The role ensures that all external partners meet rigorous regulatory standards and internal compliance requirements through assessments and continuous performance monitoring.
You join the Manufacturing Science & Technology team of an international biopharmaceutical company. Your mission is to make process data usable, visible and predictive across a portfolio of vaccine production processes. You work end to end: you structure the data, build analytics and AI tools, and deliver the dashboards process teams use every day.
Our client, a leading biopharmaceutical organization, is seeking an Analytical Scientist to join their manufacturing science and technology division. The role involves managing the transfer and validation of critical analytical methods to support the production of innovative biologics within a global manufacturing network.
Concevez, implémentez et validez des systèmes digitaux qui supportent la production GMP, garantissent l’intégrité des données et permettent des opérations efficaces et conformes dans les environnements Life Sciences.
MES Consultant – Mettre en œuvre et optimiser les MES pour soutenir une production efficace et conforme.
CSV Consultant – Valider les systèmes GxP et garantir des solutions digitales conformes aux exigences réglementaires.
MES Specialist – Configurer et maintenir les MES pour soutenir les opérations de production.
MBR Editor – Créer et mettre à jour des dossiers de lots électroniques précis.
MBR Designer – Concevoir des workflows électroniques structurés et conformes.
MBR Reviewer – Examiner et approuver les dossiers de lots électroniques pour leur exactitude.
Master Batch Editor – Maintenir et mettre à jour la documentation Master Batch.
Master Batch Reviewer – Garantir la qualité des dossiers de lots conforme aux GMP.
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