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 the supply of Vaccine and Specialty Care Biologics products. One of these two Modulus Facilities is constructed in Singapore at a new Greenfield site, with a design similar 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 Biotechnologist Intern, Manufacturing. As a member of our manufacturing operations team, you will be directly involved in running the manufacturing operations 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:

• 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 Intern, Manufacturing for the following teams:

• Upstream Manufacturing Process

• Downstream Manufacturing Process

• Central Manufacturing Services (Media & Buffer, Logistics)
  

Work Environment

• This role is based at our Modulus facility in Tuas, Singapore, requiring full-time presence on-site.

• The nature of manufacturing operations requires the need for presence on the floor to support and perform manufacturing operations.

• 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.
  

The successful applicant will be part of a 12-hour rotating shift pattern, which includes day and night shifts, including weekends. Shift allowance and company transport is provided at dedicated MRT stations to enable you to commute to and from work safely for staff working on shift. 

Performance Standards: Duties & Responsibilities

Key Areas

Action Areas, Deliverables and Outcomes

Weightage

(Total 100%)

Commissioning and Qualification Activities, Operational Readiness and Continuous Improvement projects - 10%

• 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.

• Support continuous improvement initiatives related to routine operations
  

cGMP Manufacturing Operations - 90%

• Perform and participate in the routine Product Runs in the Modulus Facility
  

Pre-requisites

Knowledge, Skills & Competencies / Language

• Self-starter with the ability to work independently while contributing effectively within cross-functional teams.

• 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 Degree in Biotechnology, Life Sciences, Chemical, Pharmaceutical Engineering, or a related field.

• Strong interest in biologics manufacturing and GMP operations.

• Willingness to work on site and 12-hour shifts.

• 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.

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