Senior Analyst, QC (Raw Materials) (ref: R2774433)

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 Modulus Facility 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 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)

About You

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.