Job Description

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.

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