
Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
Quality Expert Design & Qualification (all genders)
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.
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
The Quality Manager Design & Qualification IFF is responsible for ensuring that all aspects of Commissioning and Qualification (C&Q) activities for the project, including design, commissioning and qualification of facilities, critical utilities, equipment, and computerized systems, are executed on time and in accordance with the C&Q / Validation Master Plan, local and global requirements, and applicable regulations.
As an integral part of the project quality team, this position has overall responsibility for participating in project workstreams, ensuring proper execution of design/qualification/validation strategies as well as providing support and guidance for quality processes and procedures.
This role is expected to work independently and with a level of autonomy and authority in decision-making to ensure on-going compliance against approved documents and current Good Manufacturing Practices across the project during conceptional, basic and detailed design, construction C&Q, PQ, Validation and future site organizations until final approval.
Main responsibilities:
oversee all commissioning, qualification, and validation activities for the IFF project, ensuring compliance with plans, requirements, and regulations.
Oversee and ensure cGMP Design and IFF Quality Concepts Development and Implementation during Design Review and Design Qualification, support Process Engineering Team
Actively participate in project workstreams, providing expert guidance on quality processes and procedures.
Drive development and implementation the project's commissioning, qualification, and validation strategy, plans, and system impact assessments in collaboration with Engineering team
Prepare and execute protocols, reports, and validation master plans to maintain quality standards.
Act as Quality oversight of Supplier Qualification Engineering activities (e.g. FAT, SAT, Vendor documentation and test execution)
Foster a culture of quality compliance and continuous improvement across the project and future sites.
Collaborate with cross-functional teams to ensure quality objectives are met throughout the project lifecycle.
Provide leadership and mentorship to team members, promoting best practices in quality management.
Why choose us?:
Opportunity to work on cutting-edge projects in the biopharmaceutical industry
Collaborative and innovative work environment
Competitive salary and benefits package
Professional development and growth opportunities
Chance to make a significant impact on global health through quality management in insulin production
About you
Education/Experience: Advanced degree in Engineering, Science, Pharmacy, or equivalent field. MSc or PhD preferred; 3-5 years of industry experience in biopharma or related regulated industry,; Proven experience in Quality System Management, Process Validation Lifecycle, and Quality by Design principles
Soft and technical skills: Strong understanding of pharmaceutical manufacturing processes and GxP regulations; Expertise in quality systems, risk management, and continuous improvement methodologies; Excellent leadership, communication, decision-making, and negotiation skills; Experience with international regulatory bodies and FDA requirements; Demonstrated ability to develop and mentor team members
Languages: Proficiency in English is required; knowledge of German and French is a plus
Pursue Progress. Discover Extraordinary.
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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s 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, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
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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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