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.