INTERNSHIP DETAILS

Intern Biotechnologist

CompanySanofi
LocationSingapore
Work ModeOn Site
PostedAugust 26, 2026
Internship Information
Core Responsibilities
The intern will support commissioning, qualification, and tech transfer activities within a state-of-the-art biomanufacturing facility. They will also execute routine GMP manufacturing operations while maintaining documentation and regulatory readiness.
Internship Type
full time
Company Size
93330
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. We apply our deep understanding of the immune system to invent medicines and vaccines that treat and protect millions of people around the world, with an innovative pipeline that could benefit millions more. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives; this inspires us to drive progress and deliver positive impact for our people and the communities we serve, by addressing the most urgent healthcare, environmental, and societal challenges of our time. Interactions with this account must comply with the Terms: https://bit.ly/sanofi-terms
About the Role

About the Job 
 
Sanofi Manufacturing and Supply (M&S) Organization is preparing its future through an ambitious program named Modulus Facility. The facility is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to better address vaccine business challenges as well as Specialty Care Biologics products. One of these two Modulus Facilities is constructed in Singapore at a new Greenfield site, with a design identical to the one in Neuville (France). The facilities will also have highly digitalized and automated capabilities which is a key enabler for operations using technologies such as autonomous guided vehicles, cobots and cloud systems.  

We are seeking motivated and enthusiastic individuals for the role of Intern Biotechnologist, Manufacturing. As a member of our pioneer manufacturing operations team, you will be directly involved in Engineering and Product Validation Runs in a state-of-the-art biomanufacturing facility. This is a hands-on opportunity to contribute to core GMP operations while developing valuable technical and operational experience in biologics manufacturing. The candidate will have a routine operational role consisting of the following 

  • Perform and support commissioning and qualification activities of equipment and digital systems (e.g., automation, MES, ERP, PCS).  
  • Execute routine GMP manufacturing operations in compliance with established Process, Quality, and Safety standards.  
  • Maintain cleanliness and organization of manufacturing areas via standard housekeeping procedures.  
  • Assist in regulatory readiness activities, including documentation and audit support.  
  • Use key digital tools and automation platforms to perform manufacturing tasks and record operations.  
  • Participate in continuous improvement initiatives to optimize processes and increase operational efficiency.  

Sanofi MODULUS Singapore is hiring for Intern Biotechnologist, Manufacturing for the following teams

  • Upstream Manufacturing Process  
  • Downstream Manufacturing Process  
  • Central Manufacturing Services (Media & Buffer, Logistics)  

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.  

While we prioritize on-site work to maximize collaboration, we understand the need for flexibility. Ad hoc work-from-home arrangements can be discussed and may be approved based on individual circumstances and business needs.  

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

Company transport is provided at dedicated MRT stations to enable you to commute to and from work safely.   

  

Performance Standards: Duties & Responsibilities 
Key Areas  
1) Commissioning and Qualification Activities, Operational Readiness  
2) Tech Transfer  
3) cGMP Manufacturing Operations  

Action Areas, Deliverables and Outcomes  
1)  Perform and execute commissioning activities for manufacturing equipment and systems.  

  • Support the documentation readiness for procedures, risk assessment and other training documents for the manufacturing equipment and systems.  

2) Participate and complete all related trainings to perform the tech transfer runs.  
3) Perform and participate in the Engineering Runs and other Product Validation Runs  

 
Weightage  
1) 20%  
2) 20% 
3) 60% 

About You

Knowledge, Skills & Competencies / Language 

  • Self-starter with the ability to work independently while contributing effectively within cross-functional teams.  
  • Strong analytical and critical thinking skills, with a proven ability to navigate complex and ambiguous situations and solve problems effectively.  
  • Thrives in fast-paced, dynamic environments and is comfortable working under tight deadlines.  
  • Excellent verbal communication and presentation skills, with the ability to tailor messages appropriately for different audiences and stakeholders.  
  • Proficient in technical writing, with a clear and structured approach to documenting processes and findings.  
  • A reliable and collaborative team player who values collective success and mutual support. 

  

Qualifications / Requirement 

  • Currently pursuing or recently completed a Diploma / Degree in Biotechnology, Life Sciences, Chemical Engineering, or a related field.  
  • Strong interest in biologics manufacturing and GMP operations.  
  • Good understanding of laboratory safety and basic biotech processes.  
  • Ability to work in a team-oriented, fast-paced environment.  
  • Familiarity with digital manufacturing systems (e.g MES, ERP) is a plus.  
  • Open to shift work if required.  

 
Other requirements of the job   
Intern Biotechnologists will be required to work either:  

A 12-hour rotating shift pattern, consisting of day and night shifts, including weekends, once the facility is fully operational Or Permanent Day Shift based on operational needs and team assignments.  

Note: Shift allocation will be communicated prior to the start of the internship.  

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!

Key Skills
BiotechnologyGMP operationsTechnical writingAnalytical thinkingCritical thinkingProblem solvingMESERPAutomationBiomanufacturingCommissioningQualificationRegulatory readinessDocumentationTeam collaboration
Categories
Science & ResearchManufacturingHealthcareEngineering
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