Head of Drug Product MSAT Synthetics Platform

Head of Drug Product MSAT Synthetics Platform

Sanofi

Ambarès-et-Lagrave, France

Position Overview

The Head of Drug Product – MSAT Synthetics Platform is a senior leadership role reporting to the Head of the Synthetics Platform.

The role provides 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 across the GenMed GBU.

This role is accountable for end-to-end Drug Product performance within MSAT scope, from development through commercial manufacturing, across Sanofi’s internal sites and external partners.

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), data 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 of experience in the pharmaceutical industry, including 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 complex, global matrix organization

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 - Enables cross-functional and cross-site success
  • 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

Don't forget to mention EuroPharmaJobs when applying.

Share this Job

More Job Searches

France      Manufacturing and Logistics      On-site      Quality Assurance      Sanofi     

EuroPharmaJobs Logo

© EuroJobsites 2026