Job Description

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 Responsibilities

MES Project Lifecycle Support

Participate in the complete MES project lifecycle from initial design through build, testing, and deployment phases Assist in gathering and documenting user requirements from manufacturing and quality stakeholders Support 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 documents Participate in system build activities, including workflow configuration, recipe development, and interface setup

Testing and Validation

Support User Acceptance Testing (UAT) by preparing test scripts and executing test scenarios Assist 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 closure

System Integration and Data Management

Support integration efforts between MES and other enterprise systems (ERP, DCS, historians) Assist in data mapping, interface testing, and troubleshooting connectivity issues Help maintain data integrity and ensure accurate information flow across systems

Work Environment

This 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 / Requirement

Currently 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 advantage Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Visio)

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