Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients

Position: Quality Control Senior Analyst (Raw Material)

• Hiring Manager: Manager, QC Raw Material & Lab Service

• Location: Tuas, 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.

Sanofi has added two new Evolutive Facilities to our global industrial footprint. These production units (EVF) 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 Evolutive Facilities (EVF) will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our EVFs will help improve people’s lives by giving them faster access to more treatments.

In this context, we are looking for one Quality Control Senior Analyst (Raw Material) to support raw material testing and participate in the setting up of the new QC laboratory for our new site based in Singapore.

Main responsibilities:

• Responsible for QC test for raw material samples including compendial tests and identification tests.

• Participate in method validation/ verification for raw material testing.

• Perform QC sampling of incoming raw materials.

• Author/ revise raw material specification and other QC related documents.

• Support the laboratory start-up activities, participate in equipment qualification activities including generation of user requirement specifications.

• Support laboratory activities such as housekeeping and equipment maintenance.

• Train newcomers for QC lab activities and testing

• Participate and contribute to laboratory continuous improvement.

• Contribute to laboratory performance (eg, deviation/OOS rate, sample turnaround time)

Education and Experience

• Bachelor’s or Master’s Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 4-5 years of experience in QC lab operations and raw material testing.

• Experience in method validation/ verification in the pharmaceutical or biotechnology industry preferred.

Key technical competencies and soft skills:

• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.

• Discipline and assertiveness in decision-making and execution in laboratory start-up activities. Experienced in routine laboratory operations and continuous improvements.

• Experienced/participated in method transfer, method validation and method verification for raw material testing will be advantageous.

• Experienced in start-ups will be advantageous.

• Fluent in English speaking and writing.

Pursue Progress. Discover Extraordinary.

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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com