Head of Drug Product MSAT Synthetics Platform
About Sanofi
About the job
Position Overview
Head of Drug Product – MSAT Synthetics Platform
strategic, technical, and operational leadership
for all Drug Product (DP) activities, including:
- Formulation & Process Development
- Engineering & Maintenance (DP-related systems and equipment)
- Quality & Compliance (DP scope)
The incumbent will lead a multidisciplinary organization based in Ambarès, France, supporting a portfolio spanning
late-stage development, launch readiness, and commercial products
end-to-end Drug Product performance
Main Responsibilities
Organizational Leadership & Team Development
- Lead, develop, and inspire a multidisciplinary Drug Product organization, fostering a high-performance, accountable, and collaborative culture
- Establish and inspire a
cross - site skill area network
- Define the organizational model, capabilities, and ways of working required to deliver on current and future portfolio needs.
- Provide technical leadership and mentorship to a diverse team with expertise in pharmaceutical formulation, process development, scale-up, and manufacturing support for synthetics drug products.
- Build and sustain strong leadership within the team, ensuring succession planning and talent pipeline development
- Contribute to the Synthetics Platform's effectiveness through active participation in Global MSAT, M&S GenMed, R&D CMC Development, Industrial Product Teams, and Drug Product Manufacturing Site governance forums
Drug Product Innovation & Lifecycle Management
- Define and execute the
global DP strategy
for the synthetic product portfolio across launch, and commercialization
- Ensure robust, compliant, and efficient formulation and process development for OSD, semi-solids, liquids, and emerging formats
- Drive
platformization, standardization, and harmonization
of DP processes, formulations, and control strategies across the network
- Lead lifecycle management (LCM), including post-approval changes, cost optimization, and process improvements
- Ensure all DP activities meet
global regulatory expectations (ICH, FDA, EMA, etc.)
Commercial Manufacturing Support
- Provide end-to-end oversight of
technology transfer, validation, and commercial manufacturing support
for DP processes
- Ensure robust control strategies for
Critical Quality Attributes (CQAs)
and process performance across the lifecycle
- Lead complex troubleshooting, root cause investigations, and technical decision-making at product and network level
- Drive continuous improvement in
yield, reliability, compliance, and cost efficiency
- Ensure strong integration with MSAT transversal teams, sites, and CMOs
Innovation & Digital Transformation
- Drive innovation in
formulation science, process technologies, and manufacturing approaches
, including: Continuous Manufacturing, Advanced Characterization , Process Analytical Technology (PAT)
- Lead implementation of
digital solutions
for DP development and manufacturing: Data-driven process monitoring, Digital twins / modeling (where applicable), d ata integrity and analytics frameworks
- Build external partnerships (academia, industry) to strengthen scientific and technological leadership
Strategic Leadership & Vision
- Define and articulate a
clear vision and ambition
for Drug Product within the Synthetics Platform
- Influence enterprise-level decisions as a
trusted technical and business leader
- Contribute to the broader
MSAT and M&S strategy
, including operating model evolution
- Drive cross-functional alignment across R&D, Manufacturing, Quality, Regulatory, and Digital
- Champion change management and transformation in a complex, global environment
Key Challenges
- Managing a complex and multidisciplinary DP organization in a transforming operating model
- Driving
harmonization and standardization
across legacy processes and sites
- Delivering innovation within
resource and regulatory constraints
- Leading through
significant organizational and cultural change
- Navigating a highly matrixed stakeholder environment
About You
Basic Qualifications
- Ph.D. or advanced degree
in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or related field •
~12+ years
senior leadership roles
- Strong expertise in
drug product development and manufacturing
(formulation, process development, scale-up, validation)
- Deep knowledge of
CMC, GMP, and global regulatory frameworks (ICH, FDA, EMA)
- Proven experience with
regulatory submissions and health authority interactions
- Demonstrated ability to lead in a
Preferred Qualifications
- Experience managing broad and complex small molecule drug product portfolios
- Strong track record in
commercial manufacturing support and lifecycle management
- Experience in
digital transformation and advanced manufacturing technologies
- Demonstrated success in leading
cross-functional CMC/LCM teams
- Exposure to
continuous manufacturing, PAT, and data science applications
- Strong external network within the pharmaceutical and scientific community
Leadership Profile
Strategic & Visionary
- Translates scientific and business trends into actionable strategies
Results-Oriented
- Drives execution with accountability and measurable impact
Influential Leader
- Aligns stakeholders across complex environments
Collaborative -
Decisive
- Makes sound decisions in uncertain environments
Strategic
- Translates key business trends and scientific developments into clear, actionable plans
Continuous Improvement Mindset
- Embeds operational excellence and innovation
People Developer
- Builds strong teams and future leaders
Pursue progress , discover extraordinary
Not included in the source posting: benefits.
Skills
Who can apply
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