Role at a glance
- Salary
- Not Disclosed
- Location
- Frankfurt am Main
- Work arrangement
- On-site
- Employment
- Full-time
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About the role
Original posting provided by Sanofi
About the job
Sanofi Global MSAT (Manufacturing Sciences, Analytics, and Technology) acts as a crucial link between our R&D and Manufacturing facilities, playing a vital role in securing the present portfolio and delivering future launches of high-quality and innovative drugs and vaccines. By driving its own transformation, Global MSAT fulfils an important function by providing day-to-day Manufacturing Support, focusing on technical and process aspects, effective Life Cycle Management, process robustness enhancement, and yield improvement to optimize performance.
Join our global network and contribute to the launch of new products annually across various modalities, enabling us to reach and serve more patients and communities. Collaborate with a team of talented and passionate international experts, scientists, and project leaders who are dedicated to inventing, designing, and implementing cutting-edge industrial chemical and biological processes, analytical methods, and process modelling, all in support of Sanofi’s best-in-class ambition.
The industrialization team from the MSAT recombinant drug substance (DS) microbial platform is responsible for managing industrialization projects in the field of active pharmaceutical ingredients and acts as an interface between development and commercial production. Ready to get started?
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
Coordination and sub-project management of industrialization projects for nanobody production
Support the validation strategy for process implementation
Support technical SMEs during on-site batch execution (tech batches, Eng runs, PPQ)
Creation of GMP, regulatory, process, validation documentation in consultation with the relevant experts
Regular communication with specialist departments and operations to implement project management objectives
Creation of project documentation (e.g. schedules)
Operate as a generalist for MSAT drug substance or as a specialist in drug substance operations
Support process implementation projects, trouble shootings and best-practice exchanges
About you
Experience:
Comprehensive hands-on experience in pharmaceutical operations in industry
Experience in production and QA or QC
Experience in project management in GMP environment (e.g. validation / technology transfer projects)
Proven knowledge of GMP and regulatory affairs
Experience in microbial drug substance manufacturing is beneficial
Soft skills:
Enjoying collaboration in interdisciplinary teams
Excellent communication skills and convincing behavior
Flexibility and resilience due to a wide range of tasks
Independent and systematic working method
Excellent analytical and problem-solving skills
Strong sense of responsibility
Open and curious mindset, fostering creativity while driving for solutions and delivery
Excellent didactic skills
Technical skills:
Experience in project management tools
Experience in SAP is beneficial
Comprehensive computer skills in MS-Office
Education:
Degree (Master) in pharmacy/biology/chemistry or related disciplines
Languages:
German (proficient in speaking and writing)
English (proficient in speaking and writing)
Why choose us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Benefit from a well-thought-out benefits package that rewards your contribution and commitment.
We take care of you and your family with a wide range of health and social such as high-quality healthcare, numerous prevention programs and coverage for long-term illness. Our 14-week paid family leave for both parents is outstanding as well as a wide range of childcare benefits.
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 :€79 104,00 - €105 472Final 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.