Director - MSAT Visual Inspection
About the job
Our Team:
We are an R&D-driven, AI-powered biopharma company with one unwavering purpose: to chase the miracles of science and improve people's lives.
Our deep understanding of the immune system — combined with an innovative and growing pipeline — enables us to invent medicines and vaccines that treat and protect millions of people worldwide. At Sanofi, we believe that progress is powered by people: bold thinkers, collaborative leaders, and passionate scientists who dare to push boundaries every day.
Join us. And help change the world.
This is a great opportunity to shape the future of Visual Inspection (VI) on a global scale.
As the Director MSAT Visual Inspection Lead, you will be at the heart of Sanofi's injectable manufacturing excellence — driving the strategy, standardization, and innovation of visual inspection programs across a network of drug product sites in three Global Business Units (GBUs). You will lead a team of VI experts, champion cutting-edge inspection technologies and processes, and serve as the authoritative voice connecting Manufacturing Science, Analytics & Technology (MSAT) with Global Quality, Engineering, Procurement, and Business Strategy.
This is more than a technical leadership role — it is a platform to inspire teams, influence industry practices, and deliver meaningful impact for patients worldwide.
Main responsibilities:
• Lead the Global Visual Inspection program as MSAT authority, serving as a strategic partner in Sanofi's enterprise-wide VI strategy while aligning Global Quality, Global Engineering, Procurement, Business Strategy, and injectable manufacturing sites on all VI-related topics.
• Build, lead, and develop a high-performing team of VI experts distributed across 8 sites, providing specialist support across the full Drug Product injectable network.
• Drive global harmonization of VI strategy and implementation across Manual (MVI), Semi-Automated (SAVI), and Automated (AVI) inspection modalities for vials, pre-filled syringes, and cartridges.
• Deliver expert technical guidance on defect classification, VI recipe optimization, particulate control, false reject rate reduction, robotics, and layered inspection technologies, ensuring holistic VI lifecycle management.
• Lead the evaluation and acquisition of new VI lines and emerging technologies, ensuring full alignment with quality, regulatory, and operational requirements across the network.
• Champion innovation and industry benchmarking by identifying cost-effective inspection solutions and actively engaging with PDA, Biophorum, A3P, and other industry bodies to define and disseminate best practices across the organization.
• Ensure full regulatory compliance and good documentation practices while providing structured mentorship and knowledge transfer to develop VI capability across new and existing associates.
About you
Qualifications
Skills & Competencies
Operational & Language
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 :€100,000.00 - €133,333Final 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.