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The Digital Product Analyst supports the Digital Product team in developing integration ecosystems, engaging with stakeholders, managing Agile processes, and analyzing business requirements.
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The Senior Director leads R&D data strategy, focusing on AI and data governance to enhance portfolio decision-making, ensuring data quality and operational excellence.
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The Senior Manager, US Portfolio Marketing will develop marketing strategies for the Hemophilia Franchise and collaborate with cross-functional teams for project implementation.
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The Senior Scientist will advance drug substance development through lab automation, process engineering, and modeling, while collaborating with teams to optimize workflows using data-driven methods.
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The Senior Research Associate will lead in vivo PK/PD studies, conduct molecular assays, and oversee drug discovery research while collaborating with interdisciplinary teams.
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Manage regulatory strategies for advertising and promotional campaigns, conduct reviews of materials, and liaise with the FDA on compliance matters.
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The Product Owner leads scientific data analytics platform development, collaborating with R&D teams to innovate and streamline drug discovery processes and data analysis workflows. Responsibilities include demand management, digital product delivery, strategic planning, and performance reporting.
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The Global Submission Manager leads regulatory submissions for products, manages operational planning, and collaborates on global filing strategies. They ensure quality and compliance in the submission process and act as a Subject Matter Expert in regulatory matters.
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The Global Submission Manager oversees global submission processes, ensuring compliance with regulatory standards while managing project timelines and collaboration with cross-functional teams.
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The CMC Project Leader manages pre-clinical and early clinical development projects, leading cross-functional teams to ensure alignment and execution of CMC activities. Responsibilities include project strategy, budget management, risk assessment, and regulatory submissions.
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The Associate Scientist will develop downstream purification processes, support tech transfer, and ensure regulatory compliance during drug development.
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The Director will lead an Advanced Analytics team to improve promotional effectiveness using AI/ML models, guiding brand strategy and optimizing budgets in Sanofi's General Medicines and Vaccines Business Units.
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The Quality Control Analyst collects and records environmental and utility samples, adheres to cGMP, performs QC data reviews, and maintains lab safety. Ensures timely reporting of quality events and actively participates in investigations.
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The role involves leading advanced analytics and AI strategies for patient support services, defining product lifecycle, managing teams, and ensuring compliance with data regulations.
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As Director, Contract Analytics, you will lead complex contract analyses, manage negotiations, mentor teams, and develop pricing strategies for a major national account.
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The Digital Product Lead (Manager) is responsible for managing product roadmaps, digital product development, and analytics for patient service program integrations, while ensuring compliance and collaborating with various stakeholders.
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The Product Owner - PSPV is responsible for defining product strategy and roadmap, leading product delivery, managing relationships, and ensuring alignment with company goals, while leveraging AI and automation to enhance patient safety in the pharmaceutical sector.
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The Digital R&D Product Owner manages and optimizes digital solutions for GMP R&D labs, ensuring compliance and efficient data flows while collaborating with various stakeholders.
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The R&D Modernization Project Leader will independently lead high-impact transformation initiatives within Sanofi, ensuring strategic execution, operational excellence, and sustainable value realization across R&D operations.
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The Senior Corporate Counsel will provide legal support for biopharmaceutical manufacturing and supply transactions, collaborating with global stakeholders and enhancing operational efficiency while ensuring compliance with regulations.



