Quality Control Analyst I

Sanofi Group; Singapore; Presencial; SGD 42.000 - 64.000; Jornada completa

Descripción de la vacante

Sanofi seeks a Quality Control Analyst I (Microbiology) for our Singapore site to establish and operate a state-of-the-art QC laboratory as part of the new facility startup. You will perform microbial tests, including bioburden and endotoxin assays, and support environmental monitoring in a fast-paced GMP environment.

Ideal candidates hold a degree in Microbiology or Biological Sciences with 1–2 years of GMP laboratory experience and a meticulous, team‑oriented approach to data integrity and

Formación

• Education: Bachelor's degree or Diploma in Microbiology, Biological Sciences or related field.
• Experience: 1–2 years hands-on lab work in GMP-regulated pharma/biotech setting.
• Experience with aseptic technique and microbiology workflows is preferred.

Responsabilidades

• Perform microbiological tests (including bioburden) and endotoxin testing for water, raw materials, and product samples.
• Conduct incubation, observation, and accurate recording of test results.
• Execute environmental monitoring including viable and non-viable sampling.
• Perform water sampling (Purified water, WFI, clean steam).
• Dispense aseptic samples and maintain accurate records per GMP/data integrity.
• Write SOPs, risk assessments, and other QC documents.

Conocimientos

Aseptic technique

Microbiological testing

Environmental monitoring

Endotoxin testing

GMP and data integrity

Documentation accuracy

Teamwork/communication

Educación

Bachelor's degree in Microbiology

Diploma in Biological Sciences

Herramientas

Electronic documentation systems

Descripción del empleo

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. Sanofi has added two new Modulus Facilities to our global industrial footprint. These production units represent the future of manufacturing. They allow us to increase our capacities while making production more flexible and respectful of the environment. Fully digitalized, our Modulus Facilities will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our facilities will help improve people’s lives by giving them faster access to more treatments. In this context, we are seeking a highly motivated Quality Control Analyst I (Microbiology) to join our team and play a key role in establishing and operating a state-of-the‑art QC laboratory at our new Singapore site. This position offers an exciting opportunity to contribute to the successful start‑up of a new facility and ensure compliance with global quality standards.

Main Responsibilities

• Perform microbiological (including bioburden) and endotoxin test for water, raw materials and product samples
• Conduct incubation, observation, and accurate recording of test results
• Execute environmental monitoring activities including viable and non-viable sampling
• Perform water sampling including Purified water, WFI and clean steam
• Perform aseptic sample dispensing
• Write key documents relating to QC (such as SOPs and risk assessments)
• Maintain accurate and complete records in accordance with GMP data integrity requirements
• Actively contribute to a culture of continuous improvement and quality excellence

Education and experience

• Education: Bachelor's degree or Diploma in Microbiology, Biological Sciences, or a related scientific discipline
• Experience: Graduate or professional with 1-2 years of hands‑on laboratory experience in a GMP-regulated pharmaceutical or biotechnology setting

Key technical competencies and soft skills

• Proficiency in aseptic technique and microbiological testing
• Experience with environmental monitoring programs
• Knowledge of endotoxin testing methodologies
• Understanding of GMP regulations and data integrity principles
• Experience with electronic documentation systems
• Meticulous approach to testing, documentation, and data review
• Works effectively within a team and communicates proactively
• Thrives in a dynamic, fast-paced regulated environment
• 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! We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth.

Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.

Discover more about us visiting www.sanofi.com or via our movie We are Sanofi Start a career that makes a difference.

Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies.

Whether it’s using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.