Key Expert MSAT USP (all genders) - limited 2 years
Sanofi
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About the job
As Key Expert MSAT Upstream Processing (USP) within our MSAT Recombinant Drug Substance Microbial team, you'll develop, optimize, and transfer upstream bioprocesses for biotechnological manufacturing of peptides and proteins, specifically for our new insulin facility in Beijing. Ready to get started?
Sanofi has decided to invest into new large state-of-the art facilities for the full portfolio for insulin drug substances to ensure future oriented, sustainable, reliable and leading-edge long-term supply for world-wide diabetes patients. The new facilities will be designed as a fully automated, green, modern and state-of-the-art biologics facility considering specific process requirements of all insulins. The localization of those facilities will be in Frankfurt, Germany and Beijing, China.
You'll be part of a global MSAT Recombinant Drug Substance Microbial team spanning Germany and China, working on cutting-edge upstream bioprocessing for our transformative Beijing insulin facility project. 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, while driving innovation in biotechnological manufacturing across cultures and continents.
Main responsibilities:
● Implement and optimize upstream processes including fermentation, microbial cultivation, media preparation, and cell banking in laboratory settings for production facilities as part of interdisciplinary teams
● Optimization of separator technologies, centrifugation processes, and product recovery
● Drive scale-up activities, process characterization, troubleshooting, and manufacturing start-up operations
● Participate in technology transfer activities for upstream processes between different manufacturing sites and generate process transfer documentation
● Develop regulatory submission documents and support process validations across global facilities
● Establish and equip laboratory infrastructure and capabilities for upstream process development
● Provide technical input to regulatory dossiers and respond to authority questions regarding upstream processing
● Represent upstream processing activities in audits and inspections
● Act as the primary MSAT technical liaison, ensuring seamless sharing of expertise across the global teams.
About you
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!
The salary range for this position is :€85.572,00 - €128.340,00Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.
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PHARMACEUTICAL
Small Molecules, Biologics
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