Role at a glance
- Job function
-
Engineering & R&D Biotechnology & Pharmaceutical R&D
- Salary
- Not yet verified Check the description for pay details; an amount or pay period has not been verified.
- Location
- Frankfurt am Main
- Employment
- Full-time
- Experience
- relevant hands-on laboratory experience in upstream processing including fermentation, microbial cultivation, bioreactor operation, media development, and process scale-up, knowledge in separator operation, enzyme kinetics and protein folding beneficial
- Education
- PhD or Master's degree in Biology, Biotechnology, Biochemistry, Bioprocess Engineering, Chemical Engineering, or related field
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Role Summary
The Key Expert MSAT Upstream Processing develops, optimizes, and transfers upstream bioprocesses for biotechnological manufacturing of peptides and proteins, supporting the new insulin facility in Beijing. The role works with a global MSAT team across Germany and China.
What You'll Do
- Implement and optimize laboratory upstream processes, including fermentation, microbial cultivation, media preparation, and cell banking.
- Optimize separator technologies, centrifugation processes, and product recovery.
- Drive scale-up, process characterization, troubleshooting, and manufacturing start-up activities.
- Participate in technology transfers between manufacturing sites, prepare transfer documentation, and support process validation.
- Develop regulatory submission documents, respond to authority questions, and represent upstream processing in audits and inspections.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
PhD or Master's degree in a relevant field; relevant hands-on upstream-processing laboratory experience, including fermentation, microbial cultivation, bioreactor operation, media development, and process scale-up. Experience with cGMP environments, Design of Experiments, process modeling, PAT, and advanced process control systems; analytics expertise in HPLC, enzyme assays, gel electrophoresis, and microbiological analytical methods. Fluency in English and German, ability to work across cultures and bridge technical, manufacturing, engineering, quality, and regulatory requirements, and willingness to travel to China.
Required
- PhD or Master's degree in Biology, Biotechnology, Biochemistry, Bioprocess Engineering, Chemical Engineering, or a related field
- Relevant hands-on laboratory experience in upstream processing, including fermentation, microbial cultivation, bioreactor operation,...
- Experience with cGMP environments, Design of Experiments (DoE), process modeling, PAT (Process Analytical Technology), and advanced...
- Analytics expertise in HPLC, enzyme assays, gel electrophoresis, and microbiological analytical methods
- Strong scientific skills and ability to work across cultures and bridge technical, manufacturing, engineering, quality, and regulatory...
- Fluency in English and German, verbal and written
- Willingness to travel to China
Preferred
- Knowledge in separator operation, enzyme kinetics, and protein folding is beneficial
- Chinese language skills are advantageous
Original job description
Content provided by the employer
Original job description
Content provided by the employer
To ensure a rapid processing of your application, please apply only via the “Apply” button. Please include a letter of motivation and a current resume with your application.
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
- Education/Experience: PhD or Master's degree in Biology, Biotechnology, Biochemistry, Bioprocess Engineering, Chemical Engineering, or related field; relevant hands-on laboratory experience in upstream processing including fermentation, microbial cultivation, bioreactor operation, media development, and process scale-up, knowledge in separator operation, enzyme kinetics and protein folding beneficial
- Soft and technical skills: Experience with cGMP environments, Design of Experiments (DoE), process modeling, PAT (Process Analytical Technology), and advanced process control systems; Analytics expertise: HPLC, enzyme assays, gel electrophoresis, and microbiological analytical methods; Strong scientific skills with ability to work across cultures and bridge technical, manufacturing, engineering, quality, and regulatory requirements
- Languages/additional: Fluency in English and German (verbal and written); Chinese language skills advantageous; Willingness to travel to China, to support cross-cultural collaboration and on-site implementation activities
Pursue progress, discover extraordinary
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.
About the company
Sanofi
Large Enterprise
Sanofi is a global healthcare leader committed to promoting health and well-being through the development of innovative medicines, vaccines, and therapeutic solutions. With a diverse portfolio that spans multiple therapeutic areas, including diabetes, oncology, and immunology, Sanofi is dedicated to addressing pressing health challenges and improving patient outcomes worldwide. Headquartered in France, the company employs over 100,000 individuals across more than 100 countries, fostering a culture of collaboration and scientific excellence to drive advancements in healthcare.