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Job Title: CMC Demand & Supply Leader Location: Framingham, MA About the Job Within CMC function, in the Global CMC Project Management department, the ambition is to expand a strong End to End R&D Supply Demand integrating Demand Forecast & Planning of Supplies, supporting Projects Development and Operations through the entire value chain (from R&D to LCM). With the aim of developing a Demand & Supply Center of Excellence, the mission of the Demand & Supply Leader is to integrate Project Strategy, Clinical and CMC Operational plans for an early definition and optimization of E2E Demand & Supply plan while considering cost & risk to support execution of Projects in respect to Regulatory and Quality requirements. This role offers the opportunity to join a dynamic and skilled team at a pivotal time as we strengthen our in-house expertise, accelerate digital transformation initiatives, and build sustainable internal capabilities to support an increasing portfolio of innovative projects across multiple therapeutic areas. Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main Responsibilities • Lead collaborative work with Global project Management, Clinical Development and CMC to define clinical assumptions and CMC hypothesis to forecast Clinical Demand. • Forecast Long Range Plan Demand based on assumptions worked with interfaces. • Consolidate non-clinical & clinical demand and propagate to M&S Global Supply Chain. • Integrate all Development Demand and align with operational plans (CMC, CSO, TMED, DMPK, PCS) and Regulator submission/approval plans. • Run forecast & alignment scenario with associated risks and costs to support strategic project decisions and budget definition. • Co-lead Demand & Supply Sub Team and ensure End to End supply optimization with the contribution of key stakeholders. • Accountable for defining the best sourcing and supply strategy for marketed products/comparators, including forecast and budget. • Lead the definition of drug products blinding strategy to ensure clinical trial products indistinguishability. • Ensure DS/DP batches allocation to IMP batches and on time products delivery to packaging sites and oversee associated Material Flow & Documentation management. • Provide reporting/KPIs to monitor & improve Supply performance • Contribute to project documents & meetings preparation by providing standard Demand & Supply Reports (e.g. IDCC/DWG/ORC, IDP, Operational plan, Supply agreement). • Can support transversal initiatives contributing to simplification & harmonization. About You Basic Qualifications Education • PhD in Sciences (Neurosciences, Microbiology, Immuno-inflammation, Gene Therapy, Rare Diseases, Pharmaceutical Sciences, Biochemistry, Molecular Biology, Biotechnology, Biomedical Sciences, Genetics), Pharmacist, or Engineer in Health Sciences, Chemical Engineering, or Biomedical Engineering • OR Master of Science (MS) degree in any of the above fields • OR Bachelor of Science (BS) degree in any of the above fields • Related scientific or life sciences disciplines will be considered Experience • PhD holders: Minimum 3 years in Research and Development or Clinical Development. • Master's holders: Minimum 5 years in Research and Development or Clinical Development. • Bachelor's holders: Minimum 8 years in Research and Development or Clinical Development. • Minimum 2 years in Demand Management in Research and Development in the domain of Oncology, Immuno-inflammation, Rare Disease, Neurology, or Multiple Sclerosis (included within total years of experience, not additional) • CMC experience. • Ability to navigate complex and regulated environments (GMP and GCP regulations) • Knowledge of data analytics and forecasting • Project Management experience Preferred Qualifications • Experience in the development of diverse modalities (Mammalian, Genomic, Microbial, Synthetics) • Excellent knowledge of Projects Development, Clinical & Preclinical Development, Clinical Supply Chain, CMC, R&D and M&S interfaces • PMI certification • Experience in Power BI/Power App and project management software • Experience in management of co-development projects, companies' integration and contracts management • Knowledge of Industrial Supply Chain principles • Strong interpersonal/networking skills, team-work and transversal collaboration • Ability to understand complex processes quickly and act as referent for the department • Strong ability to work under pressure and address complex situations • Team management experience is a plus Why Choose Us • Bring the miracles of science to life alongside a supportive, future-focused team. • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. • Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs. • Help improve the lives of millions of people globally by making drug development quicker and more effective. • Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. GD-SA LI-SA LI-Onsite vhd All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.