Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
QC Analyst I / Senior Analyst II - Micro Team
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 I / Senior Analyst II - Micro Team
Hiring Manager: Team Supervisor
Location: Aventis Pharma Manufacturing, Jurong, Singapore
About the job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Ready to get started?
Roles and Responsible
- Carry out microbiological testing for APIs, stability samples, QC check of media, water and environmental samples in compliance with specifications, analytical test methods, laboratory methods and pharmacopoeia requirements.
- Prepare reagents, solutions and microbiological media 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.)
- Carry out analytical results and audit trail review.
- Assist in carrying out maintenance of laboratory equipment in compliance with established schedules.
- 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 EHS 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.
- Familiar with Pharmacopoeia such as USP, EP requirement.
About You
Jobs Requirement
- A Diploma in Microbiology or any other related scientific discipline with minimum 3 years’ experience in pharmaceutical industry.; or A fresh graduate from Degree in Microbiology 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
Why choose us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits.
Find out more about this location
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.
All-in on diversity
At Sanofi, diverse perspectives fuel the best solutions for patients. Hear from Monique Vessey, our Supply Chain Transformation Leader, on how her background shapes her approach to delivering life-changing medicines.
"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
Discover more
Manufacturing & Supply Careers
Explore how Sanofi is transforming pharmaceutical manufacturing and supply chains with cutting-edge technology, digital innovation, and sustainable practices. Discover career opportunities where you can help deliver life-changing medicines efficiently and responsibly.
Accelerating Biopharma Innovation with McLaren Racing
What do Formula 1 and biopharma have in common? Speed, precision, and a drive for excellence. Discover how Sanofi is partnering with McLaren Racing to transform drug development with cutting-edge performance science.
Join our
talent community
What could we achieve together? Every Sanofian works on projects that truly make a difference to people’s lives.
Sign up today and discover our latest opportunities as soon as they’re available.