Quality Control Analyst I
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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 !
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1065 comparable Quality roles across 134 biopharma companies.
Salary context
211 of 1065 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1065 comparable roles
+ 43 more countries
Seniority mix
524 of 1065 peers have a known seniority level
Therapeutic area mix
2 of 1065 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.