Our client, a major player in the pharmaceutical sector, is looking for an expert to drive the digital transformation of their laboratory environments. The role focuses on developing and integrating electronic laboratory notebooks to automate data flows between bioreactors, chromatography systems, and central databases.
Our client, a leading pharmaceutical organization, is seeking a Senior Manager Asset Management / Maintenance & Reliability Lead to oversee the operational asset management of production installations. This role focuses on driving enhancements in manufacturing processes while ensuring the safety, quality, and reliability of equipment and automation systems.
Our client, a leading pharmaceutical organization, is seeking a senior professional to lead validation and planning efforts for major capital projects. This role focuses on ensuring rigorous compliance with international quality standards while managing project lifecycles, product introductions, and technical coordination between departments.
Our client, a global leader in pharmaceutical R&D, is seeking a skilled Chemist to join their analytical center of excellence. The role focuses on developing innovative analytical test methods for the quantification of nitrosamines using advanced mass spectrometry techniques within a laboratory environment.
Our client, a leader in the advanced therapies sector, is looking for a professional to join their global MSAT organization. This role focuses on supporting change management initiatives for global platforms and facilitating process enhancements for innovative cell therapy technologies.
Our client, a leading pharmaceutical and medical device organization, is seeking a Project Engineer to provide technical, scientific, and project-driven support for manufacturing operations. The role focuses on leading technical improvements and sustaining on-market products through product change management and risk assessment activities.
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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