Jobs at Sanofi

负责制定并执行区域业务计划，监督与辅导医药代表的执行与学术推广，推动品牌战略落地，组织协访、招聘与培训，定期评估团队绩效并培养人才梯队，推动并践行合规文化。

Develop and apply multiscale computational models for complex diseases, ensure alignment with project team needs, and communicate modeling predictions to stakeholders.

Lead business operations for Formulation, Filling, Inspection, and Packaging at a vaccine manufacturing site. Drive schedules, capacity and headcount planning, KPI reporting, cross-functional alignment, budget oversight, strategic projects, and continuous improvement to meet production and financial targets.

Lead and oversee batch release activities to ensure GMP and regulatory compliance. Review and approve batch records and quality documentation, perform risk assessments, investigate deviations (including temperature excursions), coordinate with QC/production/regulatory, participate in audits, approve SOPs and dispositions, monitor release metrics, and drive continuous improvement and HSE integration.

Design and deliver software solutions, ensuring system scalability and reliability, while collaborating with various stakeholders to enhance data analysis and research workflows.

Join the site QA team to ensure GMP-compliant manufacturing, documentation review, audits, deviation investigations, and continuous improvement. Provide quality guidance, support corrective actions, prepare/review procedures and batch records, and participate in supplier and regulatory audits to maintain compliance.

Lead commercial strategy and execution for the vaccines portfolio in Canada. Define brand and portfolio plans, drive launch and lifecycle management, leverage market insights, manage omnichannel marketing and agency relationships, enable sales teams, engage stakeholders and public health, manage budgets/forecasts, ensure compliance, and lead cross-functional teams to deliver business growth and public health outcomes.

Drive accurate customer demand signals in Kinaxis and ERP tools by integrating statistical forecasts with local market input, consolidating forecasts, analyzing deviations, supporting S&OE and IBP meetings, identifying at-risk stock, and implementing continuous improvements to maximize forecast accuracy and OTIF.

Prepare and update global drug labeling documents and patient information for marketed and lifecycle products. Coordinate end-to-end labeling reviews, regulatory submissions, agency negotiations, approvals, and maintenance activities. Lead multidisciplinary labeling working groups, develop labeling strategies, analyze competitors, resolve cross-functional issues, and prepare responses to health authorities. Support global regulatory strategy and local affiliates while meeting submission timelines and quality standards.

Entry-level graduate position at Sanofi. The description provides limited role-specific responsibilities, emphasizing the company’s commitment to improving medications, outcomes, and scientific progress, along with diversity, equity, and inclusion.

Operate and maintain downstream vaccine processing (centrifugation, TFF, diafiltration, sterile filtration), perform sampling and area-specific testing, maintain cleanrooms and inspection readiness, execute IQ/OQ/PQ and cleaning verification, document cGMP records, support preventive maintenance, training, deviation/CAPA activities, and continuous improvement initiatives.

Plans and tracks CMC activities across pharmaceutical R&D and manufacturing, maintaining accurate timelines, dependencies, resource workloads, and high-level plans in Planisware. Conducts capacity and workload analyses, develops optimization scenarios, identifies critical paths and risks, and supports site allocation or outsourcing decisions. Coordinates with CMC project teams, regulatory, quality, finance, and global planning stakeholders in an international environment.

Lead end-to-end capital projects up to €5M for pharmaceutical manufacturing and R&D operations. Manage feasibility, design, execution, commissioning and qualification, handover, budgets, schedules, risks, resources, reporting, compliance, safety, and contractor or supplier relationships. Coordinate cross-functional stakeholders and technical interfaces within a matrix organization while ensuring adherence to GMP, FDA, construction safety, and company standards.

Leads a global regulatory affairs labeling team supporting drug development, marketed products, lifecycle management, and complex submissions. Responsibilities include hiring, coaching, resource planning, portfolio tracking, KPI management, labeling strategy, health authority responses, cross-functional consensus building, and regulatory negotiations with agencies such as FDA and EMA. Provides expert guidance on CCDS, EU, and US labeling requirements, manages complex labeling projects, develops team capability, and ensures compliant, timely labeling deliverables.

Lead oncology and immuno-oncology discovery programs from target identification through preclinical proof-of-concept. Provide scientific leadership and hands-on laboratory support, oversee translational biomarker strategies, coordinate external collaborations with CROs and academic/industry partners, and advance therapeutic modalities including small molecules, degraders, and biologics toward preclinical development.

The A2R Indirect Tax Senior Accountant will manage the Asia Indirect Tax function, ensuring compliance and providing strategic tax advice, while leading transformation projects and embracing automation technologies.

The Site Project Lead manages new production introduction projects, ensuring operational readiness and alignment with site and global stakeholders. Responsibilities include project planning, execution, risk management, and compliance oversight in line with pharmaceutical regulations.

Lead daily warehouse and logistics operations, ensuring GMP/HSE compliance, managing inventory, 3PL relationships, and production order fulfillment. Coach and develop the warehouse team, maintain SAP HANA/EWM transactions, drive continuous improvement (5S/Lean), and coordinate with internal stakeholders to meet SLAs and KPIs.

The Associate Scientist will develop downstream purification processes, support tech transfer, and ensure regulatory compliance during drug development.

Support diabetes therapeutic-area marketing and pre-launch activities: conduct market research with KOLs, develop omnichannel communication plans with cross-functional teams and agencies, monitor KPIs using CRM/AI, assist marketing plan implementation for scientific events and congresses, and prepare presentations, training materials, and logistics.