QC Analyst II

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 II (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