
Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
QC Analyst (CCP Trainee)
At a glance
Our teams produce and deliver over 4 billion units of medicines and vaccines every year, ensuring every breakthrough gets to the people who need it most.
Our state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation are redefining what’s possible: ensuring treatments reach patients faster, safer, and more sustainably than ever before. This is where your skills, ambition, and passion can shape the future of healthcare.
Job title: QC Analyst (CCP Trainee)
Hiring Manager: Quality Control Supervisor
Location: Aventis Pharma Manufacturing, Jurong, Singapore
About the Job
The Career Conversion Programme (CCP) (Train-and-Place) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme me aimed at building the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry in anticipation of hiring demand. This programme is jointly supported by the Workforce Singapore (WSG) and Workforce Advancement Federation (WAF).
The training programme consists of 15 months of local attachment at Sanofi (Aventis-Pharma). Only candidates eligible for CCP programme may apply.
Job Purpose
Carry out QC analysis in compliance with Laboratory and analytical test methods ensuring quality, cGMP, Health, Safety and environmental standards are met.
Main Responsibilities
Participate in the Daily Capacity Management and +QDCI Level 1 sessions to ensure that site and department KPI’s are met.
Carry out analytical testing for Finished Product, Intermediates, Raw Material, In-Process Control and stability in compliance with specifications, analytical test methods, laboratory methods and pharmacopoeia requirements.
Prepare reagents and solutions in compliance with GLP and laboratory SOP requirements.
Planning and assurance of cGMP compliant quality testing and documentation according to schedule. Ensure that analyses are carried out and reported in accordance with GLP (Good Laboratory Practices, completed on time and are consistent with the business requirements.
Perform analytical results review and audit trail review.
Assist in carrying out maintenance of laboratory equipment in compliance with established schedules.
Assist in carrying out on-the-job training for General Analytical Method to QC, by incorporating cGMP and safety aspects of the procedures.
Ensure GMP documents e.g. specifications, lab methods, standard operating procedures and other GMP documents (i.e. raw data, logbooks) in the laboratory are well maintained.
Responsible for electronic raw data handling in compliance with regulations and guidelines.
Participate actively in efficiency management of the laboratory and contribute towards continuous improvement through teamwork, feedback and collaboration.
Participate in regulatory inspection and customer audits preparedness at site with regards to cGMP Quality and HSE aspects.
Ensure compliance with HSE and quality policies and site procedures. Ensure safe working in the laboratory by practicing and communicating safety. Bring out unsafe conditions and acts / procedures.
Play a pro-active role in ensuring the HSE standards & Life Savings Rule are adhered to.
Embrace Zero Incident Mindset and adopt the responsible of HSE protection policies and Life Saving Rules (LSR). Practice safe laboratory operations and ensure all HSE procedures are followed.
Other responsibilities that are not included in the above but are related to quality control and in accordance with internal guidelines and SOP.
About You
A Diploma in Chemistry or any other related scientific discipline with minimum 3 years’ experience in pharmaceutical industry.; or A fresh graduate from Degree in Chemistry or any other related scientific discipline.
Must be analytical, methodical, quality conscious and a good team player.
Knowledge of FDA regulations and cGMP will be desirable.
Location: Incumbent will be based in 61 Gul Circle Singapore 629585
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
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Why work with us
- We’re problem-solvers and pioneers. United by the belief that everyone deserves a healthier future. We create best-in-class vaccines that prevent disease and protect lives.
- Innovation drives us. From AI and mRNA to next-gen science, we push the boundaries to deliver first- and best-in-class vaccines for infectious diseases worldwide.
- Growth happens here. With bold investments in R&D and world-class facilities, Sanofians across the entire vaccine lifecycle are shaping the future of global health.
- We do what’s right. Sustainability and DE&I drive our positive global impact—because the diverse communities Sanofians represent are the patients we serve.
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"Manufacturing and Supply is the bridge between the science that happens in research laboratories and the people and communities we serve."

Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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