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.

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!