MES Engineer Intern

Sanofi Manufacturing and Supply (M&S) Organization is preparing its future through an ambitious program named Modulus Facility. The facility 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 the supply of Vaccine and Specialty Care Biologics products. One of these two Modulus Facilities is constructed in Singapore at a new Greenfield site, with a design similar 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, cobots and cloud systems.We are seeking a motivated and technically skilled MES Engineer Intern to join our Smart Factory team in Tuas, Singapore. This internship offers a unique opportunity to gain hands-on experience in implementing and optimizing Manufacturing Execution Systems within a highly-digitalized pharmaceutical manufacturing facility. You will work alongside experienced engineers and cross-functional teams to support the design, build, and testing phases of MES projects that directly impact our production capabilities.Key ResponsibilitiesMES Project Lifecycle SupportParticipate in the complete MES project lifecycle from initial design through build, testing, and deployment phasesAssist in gathering and documenting user requirements from manufacturing and quality stakeholdersSupport the configuration and customization of MES modules including production management, material tracking, quality management, and electronic batch records (EBR)Contribute to the development of functional specifications and technical design documentsParticipate in system build activities, including workflow configuration, recipe development, and interface setupTesting and ValidationSupport User Acceptance Testing (UAT) by preparing test scripts and executing test scenariosAssist in the validation process in accordance with pharmaceutical industry standards (FDA 21 CFR Part 11, EU GMP Annex 11)Document test results, identify system issues, and track resolution through to closureSystem Integration and Data ManagementSupport integration efforts between MES and other enterprise systems (ERP, DCS, historians)Assist in data mapping, interface testing, and troubleshooting connectivity issuesHelp maintain data integrity and ensure accurate information flow across systemsWork EnvironmentThis role is based at our Modulus facility in Tuas, Singapore, requiring full-time presence on-site.While we prioritize on-site work to maximize collaboration, we understand the need for flexibility. Ad hoc work-from-home arrangements can be discussed and may be approved based on individual circumstances and business needs.Qualifications / RequirementCurrently pursuing or recently completed a Degree in Biotechnology, Life Sciences, Chemical, Pharmaceutical Engineering, or a related field.Strong interest in biologics manufacturing and GMP operations.Knowledge of programming or scripting languages would be an advantageProficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Visio)nullPursue Progress. Discover Extraordinary.Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.