Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
Scientist II (Upstream), MSAT
At a glance
Our teams produce and deliver over 4 billion units of medicines and vaccines every year, ensuring every breakthrough gets to the people who need it most.
Our state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation are redefining what’s possible: ensuring treatments reach patients faster, safer, and more sustainably than ever before. This is where your skills, ambition, and passion can shape the future of healthcare.
Overview
Manufacturing Sciences, Analytics and Technology (MSAT) drives the industrialization and continuous improvement of biological processes and products. The function embraces new technologies and digital innovations while serving as the custodian of manufacturing process knowledge.
Positioned at the intersection of R&D and manufacturing, MSAT is a multidisciplinary function providing expertise in process sciences, manufacturing, process modelling, statistical analysis, validation, and technology transfer.
The Scientist II, Upstream MSAT Laboratory (Modulus Singapore) is responsible for independently designing and executing laboratory studies to support manufacturing troubleshooting, technology transfer, and lifecycle management for commercial biologics production. The role also contributes to the evaluation of emerging and innovative technologies, including automation.
Working closely with MSAT process engineers, this position translates manufacturing challenges into robust laboratory study designs, authors protocols and reports, and executes experiments with scientific rigor. The role operates with a high degree of autonomy, under the strategic guidance of the MSAT Laboratory Manager, and may require flexible working hours, including after-hours support when needed.
Key Responsibilities
1. Laboratory Studies & Scientific Execution
Design and execute small- to mid-scale upstream laboratory studies supporting manufacturing investigations, technology transfer, and process improvements.
Collaborate with MSAT process engineers to define study objectives and develop robust experimental designs.
Author study plans, protocols, reports, and technical documentation in compliance with GLP standards.
Analyze and interpret experimental data, draw scientifically sound conclusions, and present findings to cross-functional stakeholders.
Ensure all laboratory activities are conducted safely, within scope, and on schedule.
2. Manufacturing Support & Troubleshooting
Provide upstream scientific expertise to support manufacturing investigations.
Design and execute studies for root cause analysis and CAPA development.
Support urgent and time-sensitive activities, including flexible hours or weekend work where required.
Contribute to after-hours support for critical manufacturing issues.
3. Laboratory Operations
Maintain laboratory readiness, including equipment setup, cleaning, maintenance, and coordination with vendors and engineering teams.
Manage inventory of materials and consumables, including procurement and stock monitoring.
Maintain accurate laboratory documentation (e.g., logbooks, inventory records) and ensure compliance with GLP and HSE standards.
Review and approve operational documentation to ensure compliance.
4. Technology Transfer Support
Support technology transfer activities through execution of laboratory studies (e.g., scale-down model qualification, bridging studies).
Contribute to drafting and compilation of technology transfer documentation.
Promote standardization and knowledge management practices within the site and global network.
5. Lifecycle Management & Continuous Improvement
Analyze laboratory and manufacturing data trends to identify improvement opportunities.
Support process optimization and continuous improvement initiatives.
Stay updated on industry trends and emerging upstream technologies, recommending enhancements where appropriate.
Author documentation supporting change management, including risk assessments and mitigation strategies.
6. Mentorship & Team Contribution
Mentor trainees and interns on laboratory techniques, scientific thinking, and GLP practices.
Contribute to a collaborative and high-performance laboratory environment.
Requirements
Core Competencies
Strong communication skills in cross-functional and multicultural environments.
Solid analytical and problem-solving capabilities with a data-driven mindset.
Self-motivated and able to work independently with minimal supervision.
Scientifically curious with a continuous improvement mindset.
Proficiency in Design of Experiments (DOE) and statistical analysis tools.
Familiarity with Process Analytical Technology (PAT) and monitoring tools.
Technical & Educational Background
Advanced degree in Biological Sciences, Biotechnology, Chemical Engineering, Chemistry, or related field.
Hands-on experience in biopharmaceutical laboratory environments, with demonstrated ability to independently design and execute studies.
For upstream specialization:
Experience in mammalian cell culture (seed train to bioreactor systems)
Familiarity with relevant analytical techniques
Strong understanding of process parameters and their interactions in upstream processes.
Experience with scale-down model development and/or qualification is highly desirable.
Familiarity with HSE, GLP, and basic cGMP requirements in biopharmaceutical environments.
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
Final compensation will be determined based on factors such as experience, skills, expertise, location, and others. Employees may be eligible to participate in company employee benefit programs.
Find out more about this location
Why work with us
- We’re problem-solvers and pioneers. United by the belief that everyone deserves a healthier future. We create best-in-class vaccines that prevent disease and protect lives.
- Innovation drives us. From AI and mRNA to next-gen science, we push the boundaries to deliver first- and best-in-class vaccines for infectious diseases worldwide.
- Growth happens here. With bold investments in R&D and world-class facilities, Sanofians across the entire vaccine lifecycle are shaping the future of global health.
- We do what’s right. Sustainability and DE&I drive our positive global impact—because the diverse communities Sanofians represent are the patients we serve.
All-in on diversity
At Sanofi, diverse perspectives fuel the best solutions for patients. Hear from Monique Vessey, our Supply Chain Transformation Leader, on how her background shapes her approach to delivering life-changing medicines.
"Manufacturing and Supply is the bridge between the science that happens in research laboratories and the people and communities we serve."
Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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