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Location
In office (Singapore)
Employment
Full-Time
Overview
Company
Impact
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Sanofi is a French pharmaceutical company formed in 1973 and assembled over five decades through a long series of mergers including Synthelabo, Aventis and Genzyme. It is now built around immunology and rare disease, with Dupixent for atopic dermatitis and asthma as by far its largest product, alongside a substantial vaccines division covering influenza, meningitis and the respiratory syncytial virus antibody Beyfortus. Headquartered in Paris, the group has sharpened its focus in recent years by separating its consumer healthcare business into the standalone company Opella and directing research spending toward biologics and immune science.

The MES Engineer sits within the Site Engineering & Maintenance Department and is responsible for the implementation, maintenance, optimisation and lifecycle management of the site Manufacturing Execution System (MES) and associated integrations.

Acting as the Business System Owner (BSO) and technical SME for MES, the role ensures that the system remains reliable, compliant and fit for manufacturing needs while supporting system enhancements, IoT device integration, site projects and digitalisation initiatives.

Main Accountabilities

  • Act as the Business System Owner (BSO) and SME for MES, leading system configuration, maintenance, upgrades and continuous improvement to support manufacturing requirements.
  • Develop and maintain MES system architecture, databases, Process Instructions and technical specifications, ensuring alignment with global design standards and site requirements.
  • Maintain and optimise interfaces and connectivity between MES and other site systems, including integration of relevant IoT devices and digital solutions.
  • Provide advanced technical support, troubleshoot complex MES issues and collaborate closely with the Digital team and system vendors to ensure timely resolution and minimise system downtime.
  • Lead the implementation of MES-related activities arising from site projects, change controls, deviations and CAPAs, providing technical expertise from design through commissioning and operational handover.
  • Support the Computerised System Validation (CSV) lifecycle, including validation activities, system changes, documentation and maintenance of the validated state.
  • Ensure MES remains compliant with GMP, data integrity, cybersecurity and applicable regulatory requirements, including appropriate user access, security controls, system backup and recovery processes.
  • Serve as the MES SME during regulatory inspections, internal audits and self-inspections, supporting documentation, investigations and remediation activities as required.
  • Monitor system performance, downtime and deviations, identify recurring issues and drive improvements to enhance system reliability, operational efficiency and user experience.
  • Develop and maintain relevant SOPs, technical documentation, system specifications and engineering records in accordance with site Quality and Engineering standards.
  • Provide technical training and ongoing support to operations and end users, ensuring appropriate understanding and use of MES functionalities.
  • Manage MES system vendors for technical support, troubleshooting, maintenance and project execution, including review of technical proposals and vendor documentation.
  • Participate in global MES and digital networks, sharing lessons learned and supporting global initiatives while ensuring alignment with global standards and design guidelines.

Key Decision / Advisory Responsibilities

The MES Engineer will have responsibility for determining appropriate system configurations and technical optimisation strategies, while providing expert advice on troubleshooting, system performance and technical solutions. The role will monitor and report MES downtime and deviations, contribute technical expertise throughout the validation lifecycle, and support compliance documentation, inspections and continuous improvement activities.

Key Interfaces

The role will work closely with Manufacturing, Engineering & Maintenance, Digital/IT, Automation, Quality, Validation, Global MES teams and external system vendors to ensure reliable, compliant and effective operation of the site's MES environment.

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

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