Activités Industrielles
Là où les miracles
de la science
deviennent une réalité pour les patients
Senior Engineer I, MSAT
En bref
Nos équipes produisent et livrent chaque année plus de 4 milliards de médicaments et de vaccins, veillant à ce que chaque avancée soit accessible à ceux qui en ont le plus besoin. Grâce à des infrastructures ultra-modernes, des usines intelligentes pilotées par l’IA et une automatisation de pointe, nous repoussons les limites pour garantir que nos traitements parviennent aux patients plus rapidement, en toute sécurité et de manière plus durable que jamais. C’est ici que votre expertise, votre ambition et votre passion peuvent façonner l’avenir de la santé.
Job title: Senior Engineer I, MSAT
Location: Singapore
Hiring Manager: Head of Manufacturing Technology
About the job:
Purpose
Sanofi Manufacturing and Supply Organization is preparing its future through an ambitious program named Modulus. The EVF Project is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable and agile, leveraging new disruptive technologies, to better address vaccine business challenges as well as Specialty Care biological products. One of these two Modulus is implemented in Singapore in a new Greenfield site, with a design similar to the one in Neuville (France). Our manufacturing sites are state-of-the-art, powered by big data and digital. It is the bridge between scientific advances and transformative medicines and will be serving millions of people around the world.
Manufacturing Science and Analytical Technology (MSAT) drives the industrialization and the improvement of biological processes and products. It embarks new technologies and digital trends. It is the keeper of manufacturing process knowledge. MSAT is at the crossroad of R&D and production. It is a multi-disciplinary function that provides expertise in process, manufacturing sciences, process modeling, statistical analysis, process validation and technology transfer.
The MSAT team in Sanofi Modulus Singapore is seeking a downstream Senior Engineer I to provide technical expertise for downstream biological process areas in various activities like new product introduction, technology transfer, shopfloor support and troubleshooting activities at manufacturing scale, as well as lead process investigations. The MSAT Senior Engineer I is expected to lead deviations & CAPA plans, and can be consulted by Manufacturing leads for equipment & operational workflows. This role can specialize to become a network SME/KOL.
Duties & responsibilities
Process transfer & validation
• Downstream SME to provide scientific/technical expertise including process equipment, process mass balances, process validation and process design & control.
• Work closely with receiving unit MSAT DS leads as well as sending unit teams to facilitate technology transfer of new molecules, including defining manufacturing processes and workflows, establishing strategies behind process validation and process control.
• Author downstream MSAT technical documents (e.g. memos, protocols, reports, plans) during process transfer & validation phase and process monitoring.
• Build and promote systems and tools for (i) standardization concepts & implementation, (ii) sharing and retention of design knowledge, within site and Sanofi network.
Manufacturing support
• Provide downstream MSAT technical perspective and main author for MSAT documentation in downstream process situations such as change controls, impact assessments and memos.
• Provides consultation to manufacturing coworkers from scientific and technological perspectives.
• In process disruptions, serve as secondary shopfloor escalation contacts, including leading process risk/gap assessments, investigations, change controls & CAPA implementation. Is part of after-hours MSAT on-call system to support manufacturing disruptions.
Molecule lifecycle management & yield improvement activities
• Identify trends, assess potential causes and propose & own improvement activities, including working cross-functionally within the site and network.
• Support/Lead site-level projects involving key process changes.
• Develops downstream MSAT technical documents during process improvements.
• Is (or work towards) a domain expert at site, or network key opinion leader.
• May mentor junior coworkers.
About You
Pre-requisites
Knowledge, Skills & Competencies / Language
• An effective communicator and productive in multi-functional & multi-cultural communication settings.
• Has excellent analytical, consultative and diagnostic skills with ability to make sound, data-based business decisions.
• Self-directed and comfortable working with a high level of autonomy, for initiating activities to close gaps and complete assigned tasks.
• Data-driven and scientifically curious.
Qualifications/ Requirements
• Holds a scientific or engineering degree (or higher), preferably in Biotechnology, Biological Sciences, or Chemical Engineering.
• Has more than 5 years of broad industrial experience in biopharmaceutical projects, particularly in technology transfers, process validation and/or manufacturing support.
• Possesses strong understanding of critical processes/operations as well as interactions between different process parameters.
• Has hands-on experience in pilot-scale or large-scale facilities, of cell culture and/or purification techniques.
• Is familiar with cGMP concepts in biopharmaceutical environments and up-to-date with regulatory requirements and industry best practices.
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Pourquoi nous rejoindre ?
- Nous ne faisons pas que fabriquer des médicaments—nous créons un impact. Grâce à notre réseau international d’installations de pointe, nous veillons à ce que les patients reçoivent les traitements dont ils ont besoin, au moment où ils en ont besoin.
- L’innovation est notre moteur. De la fabrication pilotée par l’IA aux méthodes de production inédites, nous repoussons les limites de l’efficacité et de la performance.
- Ici, vous évoluez. Que ce soit en production, en qualité, en ingénierie ou en supply chain, vous collaborerez avec des experts de renom, développerez vos compétences et contribuerez à façonner l’avenir de l’industrie pharmaceutique.
- Nous faisons ce qui est juste. Sécurité, durabilité, diversité, équité et inclusion sont au cœur de notre engagement, garantissant un environnement où chacun peut s’épanouir.
Tous engagés pour la diversité
Chez Sanofi, la diversité des perspectives est une source d’innovation au service des patients. Découvrez Hamza Laajaj, Chef de projet déploiement applicatif à Neuville-sur-Saône, et son engagement pour un environnement inclusif où chaque voix compte. Pour lui, c’est en embrassant la diversité que nous libérons l’innovation et repoussons les limites de la santé.
"Nous faisons ce qui est juste. Sécurité, développement durable, diversité, équité et inclusion sont au cœur de notre engagement, garantissant un environnement où chacun peut s’épanouir."
Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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