
Supply Chain Operations Specialist Trainee – Sanofi Tuas
Location: Tuas, Singapore
Job Type: Career Conversion Programme (CCP) (15 Months)
Department: Supply Chain & Logistics
About Sanofi
We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.
About the Job
As a Supply Chain Operations Specialist within our Supply Chain & Logistics team at Sanofi Tuas, you will play a critical dual role – combining GMP-compliant quality sampling operations with hands-on warehouse and logistics responsibilities.
This is an exciting greenfield opportunity in a dynamic, fast-paced pharmaceutical manufacturing environment where you will contribute to building robust processes from the ground up.
Sanofi's Tuas site is a state-of-the-art, greenfield pharmaceutical manufacturing facility in Asia Pacific, dedicated to producing life-saving medicines that reach patients around the world. In this combined role, you will ensure that raw materials, single-use technologies, and consumables are accurately sampled, documented, received, stored, and dispatched – all in full compliance with cGMP, GDP, and Sanofi quality standards. You will be at the heart of our mission, directly supporting manufacturing quality, regulatory compliance, and supply chain continuity.
Main Responsibilities
Perform sampling of raw materials in strict accordance with approved SOPs, sampling plans, and GMP requirements
Apply validated sampling techniques and equipment (e.g., sampling thieves, scoops, syringes) to ensure representative samples while minimising contamination risks
Accurately label, document, and segregate samples, including batch numbers, dates, quantities, and storage conditions
Conduct visual inspections during sampling and report any deviations, abnormalities, or out-of-specification (OOS) observations immediately to the supervisor
Lead or contribute to investigations of sampling-related deviations, OOS results, or complaints, including root cause analysis and CAPA implementation
Maintain sampling records, logbooks, and electronic systems (e.g., LIMS, SAP, or equivalent) in full compliance with ALCOA+ data integrity principles
Ensure personal hygiene, room disinfection, gowning, and ongoing training compliance for all GMP-regulated areas
Warehouse Operations
Inventory & Documentation Management
Compliance & Quality Standards
About You
Education
Skills & Competencies
Physical Requirements
Why Choose Us?
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!

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.
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