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Sanofi is seeking a Supervisor, Manufacturing in Tuas, Singapore to lead startup and operations for engineering and PPQ batches within a modern, digitalized facility. You will oversee a team of biotechnologists, ensure GMP compliance and safety, and drive continuous improvement across manufacturing processes.
The role requires a university degree with substantial experience, plus leadership in a GMP environment and familiarity with DeltaV/MES systems.
Hiring Manager: Manager, Manufacturing
Location: Tuas, Singapore
Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus 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 Biologics products. One of these two Modulus is implemented in Singapore in a new Greenfield site, with a design identical to the one in Neuville (France). The facilities will also have highly digitalized and automated capabilities which is a key enabler for operations using technologies such as autonomous guided vehicles (AGVs), cobots and cloud systems. The manufacturing team in Sanofi Modulus, Singapore is seeking to expand the team and has an open position as Supervisor, Manufacturing, responsible for the operations in either Central Manufacturing Services (CMS) or Process Manufacturing (PM) team. The role will report to the Manager, Manufacturing. In this role, you will be responsible to lead the startup and operation of the manufacturing areas to produce engineering and PPQ batches with the aim of commercial production. In line with this, you will be responsible to provide field leadership to the team of biotechnologist who will be your direct reports. The working hour of this role is 12-hour rotating shifts (day and night) and also include weekends and public holidays. The Supervisor, Manufacturing will (not limited to the following): Ensure compliance with GMP, safety regulations, and company procedures. Train, develop, and evaluate team members' performance. Troubleshoot equipment and process issues. Maintain accurate production records and documentation. Initiate and implement continuous improvement initiatives. Manage inventory and resource allocation in the manufacturing operations. Collaborate closely with cross functional teams to operate the manufacturing process manufacturing process lifecycle and supporting deviation investigations line including management of changes and CAPA implementation, management As a fronter or Subject Matter Expert (SME) to support the team for regulator inspection audits.
Key Areas Action Areas, Deliverables and Outcomes Weightage (Total 100%) Team Management and Leadership 50% Hire, train and manage direct team reports. Manufacturing Operations 50% Lead and perform operations on the production floor. Ensure compliance to applicable HSE and quality guidelines.
Pre-requisites Knowledge, Skills & Competencies / Language Team management Self-starter and independent worker who can operate and perform in cross functional setting. Possess analytical and critical thinking skills with the ability to problem solve and navigate through complexity and ambiguity. Able to work in fast paced and dynamic conditions with tight timelines. Excellent analytical, consultative, and diagnostic skills with ability to make sound, data-based business decisions. Effective communication skills necessary to interact with internal stakeholders (includes strong presentation skills). Good technical writing skills.
University Degree or equivalent with at least 8 years of relevant experience. Biotechnology/Pharmaceutical with At least 2 years of people leadership experience in Manufacturing area. Experience with cGMP documentation and record maintenance. Strong troubleshooting, problem solving and prioritization skills are required. Familiarity and prior working experience with Single Use Systems would be preferred. Previous work experience in a digitalized and automated facility operated by DeltaV and MES would be preferred.
Diversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden. Wir sind ein forschendes Biopharma-Unternehmen, das KI anwendet und sich dafür einsetzt, das Leben der Menschen zu verbessern und verantwortungsvoll zu wachsen. Unser Team wird von einem Ziel geleitet: Wir erforschen die Wunder der Wissenschaft, um das Leben der Menschen zu verbessern. Wir möchten eine gesündere, widerstandsfähigere Welt schaffen und das Unmögliche möglich machen, indem wir Medikamente und Impfstoffe für Millionen von Menschen weltweit entdecken, entwickeln und bereitstellen. Erfahren Sie mehr über uns auf www.sanofi.com oder schauen Sie sich unseren Film an: We are Sanofi Starte eine Karriere, die einen Unterschied macht. Neuerfindung liegt in unserer DNA. Sie hat unsere Entwicklung von einem kleinen französischen Unternehmen zu einem der weltweit führenden Biopharma-Unternehmen vorangetrieben. Ob es darum geht, KI zu nutzen, um die Zeiten der Arzneimittelforschung zu verkürzen, oder Vertrauen im Gesundheitswesen aufzubauen – du kannst unseren Teams dabei helfen, das Leben für Patient*innen, Partner*innen und Gemeinschaften zu verbessern. Hier entwickelst du deine Karriere weiter. Wir öffnen dir die Tür, um neue Möglichkeiten zu entdecken, deine Grenzen zu erweitern und dich mit Menschen zu vernetzen, die von einem gemeinsamen Ziel angetrieben werden: Wir erforschen die Wunder der Wissenschaft, um das Leben der Menschen zu verbessern.