Quality Control Analyst I

Sanofi is hiring a Quality Control Analyst I. Level rates it ; you can apply on Sanofi.

Level's read on this job

Level rates this role Little AI ●○○○: aI is not part of the work.
Tools and skills the posting cites include Gmp Systems, Laboratory Equipment and microbiology.
Level classifies it as a junior role.
Level lists 1,000+ other open roles at Sanofi.

AI in this role

Perform microbiological testing and environmental monitoring to ensure quality and compliance at Sanofi's manufacturing facility.

Gmp SystemsLaboratory Equipment

microbiologyquality-controlgmpaseptic-technique

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!

How we rate this

Quality Control Analyst I at Sanofi rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

●●●● Builds AI80 to 100
●●●○ Works on AI60 to 79
●●○○ Uses AI40 to 59
●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Key facts

Quality Control Analyst I is an open job at Sanofi.
Level rates this role AI Level 1 of 4: Little AI.
The role is based in City of Singapore.
The job was posted on September 1, 2026.
Seniority: junior.
Applications are handled by Sanofi. Apply on Sanofi

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

MicrobiologyQuality ControlGmpAseptic TechniqueGmp SystemsLaboratory Equipment

Questions you could be asked

Tell me about a project where microbiology was part of your work. What did you do?
Tell me about a project where quality control was part of your work. What did you do?
Tell me about a project where gmp was part of your work. What did you do?
Tell me about a project where aseptic technique was part of your work. What did you do?
Walk me through how you've used Gmp Systems in your day-to-day work.

Adapt your resume

List these exact terms on your resume: Microbiology, Quality Control, Gmp, Aseptic Technique, and Gmp Systems. An applicant tracking system matches the wording, not the idea.
Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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