Validation Engineer Intern

**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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