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Trouvez votre prochain poste en Regulatory Affairs dans les Life Sciences et contribuez à garantir un accès au marché conforme et une excellence réglementaire au sein des principales entreprises de Belgique.
Our client, a leading pharmaceutical organization, is looking for a specialist to provide data stewardship and process ownership for its regulated content and regulatory information. This role focuses on supporting end-users and managing diverse product portfolios through effective database management and training.
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 organization, is looking for a Quality SME to support a significant capacity expansion project at one of their sites. This role ensures that engineering processes and equipment systems comply with regulatory standards from the design phase through to operational release.
Our client, a leading organization in the pharmaceutical industry, is seeking a MES Quality Engineer to join their supply chain quality team. The role focuses on providing quality oversight and ensuring the compliant release of pharmaceutical products within a specialized production environment.
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.
We are looking for a Warehouse QA Officer who is a team player and customer oriented to join our Pharma & Injectable Quality department.
Our client, a leading pharmaceutical organization, is seeking a Reference Standard Owner to support a highly regulated production environment. This role involves managing the full lifecycle of assigned reference standards, ensuring all qualification and requalification activities meet stringent quality standards and project timelines.
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.
Que vous soyez spécialisé en stratégie réglementaire, conformité ou étiquetage : nous proposons des postes variés dans le secteur Life Sciences.
Regulatory Strategist – Définissez et pilotez la stratégie réglementaire tout au long du cycle de développement.
Expert en affaires réglementaires – Assurez le suivi complet des dossiers réglementaires, de la soumission à l’après-approbation.
Spécialiste Regulatory Affairs – Veillez à la conformité des produits pharmaceutiques avec les réglementations belges et européennes.
Consultant Artwork & Labeling – Gérez les processus d’étiquetage et contrôlez les éléments visuels selon les exigences réglementaires.
Spécialiste en étiquetage – Garantissez l’exactitude et la conformité des informations produits sur tous les marchés.
Consultant CMC Regulatory Affairs – Préparez les dossiers réglementaires liés à la qualité, fabrication et contrôle (CMC).
Coordinateur de projets réglementaires – Coordonnez les projets, échéances et communications avec les parties prenantes.
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