Quality Management System Specialist - VIE Contract

• Location: China, Beijing
• Target start date: 01/03/2026

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.

About the job

As Quality Management System Specialist VIE within our Quality team, you will play a critical role in establishing and maintaining a robust Quality Management System (QMS) that meet Food and Drug Administration (FDA), European Medicines Agency (EMA), and Chinese Pharmacopoeia regulations while implementing state-of-the-art Current Good Manufacturing Practices (cGMP) design and qualification/validation processes. Ready to get started?
 

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

About Sanofi

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

• Ensure project compliance with Sanofi Standards and Good Practices.
• Establishing and maintaining a robust Quality Management System (QMS).
• Provide Quality oversight.
• Support quality project cost tracking and ensure schedule compliance.

About you

Experience:

• Interest or first experience in global project work and multicultural collaboration.

Soft and Technical skills:

• Understanding of QMS systems, Process Validation Lifecycle, and Quality by Design.
• Knowledge of biologic product license application process and regulatory requirements.
• Problem-solving mindset.
• Willingness to adapt to new cultural environments.
• Open to relocation and excited to experience life and work in China.

Education:

• Master’s degree in Science or Pharmacy with Quality focus.

Languages:

• Fluent English (written and verbal).
• Mandarin or German would be a plus.

Why choose us?

• Be part of a pioneering biopharma company where patient insights shape drug development.
• Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
• Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
• Transform lives worldwide by delivering life-changing treatments anywhere, anytime.
• Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.
• Every year, we distribute over 4 billion units of medicines and vaccines, ensuring people worldwide receive the treatments they trust.