Sanofi

MES Engineer/Specialist

Singapore · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

EmployerSanofi
LocationSingapore
Work styleWork style not stated
Employment typeFull time
Employer posted23 Sep 2026

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.

Show full description

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!

See how well you match this job Apply on the employer’s site ↗

Check your resume against this job Free, no sign-up. Nothing you paste is stored.

Staying safe while you apply

Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
Prepare honestly.
Build interview stories and application drafts from your own evidence.
Keep track.
Save the role and record your own application status and follow-ups.

Create a free workspace or log in.