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Validation Engineer Intern

Synthorx

Synthorx

Singapore
Posted on Oct 1, 2025

Job title: Validation Engineer Intern

  • Reporting To: Senior Manager, Validation

  • Location: Tuas, Singapore

Within the Modulus Manufacturing Facility, the Validation Engineer (Intern) participates in setting up and running the validation lifecycle management program for the facility in Tuas. He / She will be working closely with engineering, manufacturing, safety and quality teams to implement a lean, compliant and efficient validation program.

Key accountabilities

  • Create Standard Operating Procedures (SOP) and training materials for Validation Lifecycle Management

  • Lead / execute validation activities as part of the site start up activities.

  • Create an efficient system / mechanism to generate the annual validation plan / report for GxP system

  • Design and implement qualification and validation template / SOP to standardize and support the best way of working for more routine requalification activities

  • Develop validation deliverables including risk assessments, system impact assessments, requirement traceability matrix, validation plans, protocols and reports

  • Ensure compliance with cGMP as well as all Sanofi Quality requirements.

Skillsets Expected

  • Innovation skills in project and production environment / Think out of the box

  • Ability to work in multi-disciplinary and multicultural team / Excellent communication ability / Team spirit

  • Self-starter, proactive, self-organized and Independent

  • Excellent analytical, consultative, and diagnostic skills with ability to make scientific, data driven decision

  • Proficient in spoken and written English, with a keen eye for detail

Work Environment

  • This role is based at our Modulus facility in Tuas, Singapore, requiring full-time presence on-site.

  • The nature of manufacturing operations and the importance of face-to-face collaboration with various stakeholders necessitates working from our facility to ensure optimal team performance and operational excellence.

  • Typical work hours for this role are from 7.45am to 4.45pm, Monday to Friday.

Education and experience

  • Currently pursuing Bachelor’s Degree in Engineering or Biological Sciences.

  • Good knowledge of biopharmaceutical knowledge and basic understanding of GMP

  • Prior experience (including internships) in a manufacturing facility will be an advantage.

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.

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