Jobs at Sanofi

The Head of US Litigation and Investigations leads and oversees litigation and investigations, managing risks and costs while providing strategic direction. Responsible for external counsel management, budget oversight, and cross-functional collaboration within the healthcare and pharmaceutical sectors.

Lead a 40-person team across pricing, contract development, analytics, and operations for the US vaccines portfolio. Develop and implement US launch and in-line list/net pricing strategies, government pricing compliance, innovative contracting aligned to health economic models, and long-term pricing/contract strategy. Oversee offer development, competitive landscape evaluation, negotiations, agreement execution, performance measurement, and pricing systems.

Serve as the finance lead for Global Immunology franchise, driving P&L, forecasting, budget, launch finance, strategic planning, investment analysis, and investor relations while partnering with R&D, commercial, supply chain, and global stakeholders to support decision-making and resource allocation.

Provide strategic leadership enablement by coordinating executive workflows, AI-enabled productivity, and transformation workstreams. Prepare executive briefings and communications, manage governance and meeting rhythms, drive program delivery, and support stakeholder engagement, travel, and operational executive support to increase leadership capacity and execution.

Develop and validate biochemical and biophysical analytical methods to characterize mRNA vaccine drug substances/products (primarily LC-MS). Support CMC activities, write method documentation and regulatory reports, execute complex experiments, assist QC/CRO investigations, participate in GMP/non‑GMP lab setup, train junior staff, and ensure quality and safety compliance.

The Device Quality Engineer leads global processes for device risk management and compliance, ensuring adherence to regulations, analyzing post-market data, and collaborating with cross-functional teams.

Manage the Three‑year One Sanofi Leadership Development Program, coordinating rotations (first in Sales) across commercial and related functions. Support strategy, pricing, market research, forecasting, financial valuation, and business development activities while developing leadership skills and driving brand and portfolio initiatives across Specialty Care, Vaccines, or General Medicines.

Perform GMP-compliant large-scale biopharma manufacturing tasks including operating and preparing equipment, CIP, batch record review, documenting deviations, troubleshooting basic mechanical issues, maintaining clean production areas, and training or leading other operators. Follow procedures, complete production documentation, and use Microsoft Office; may use/learn Manufacturing Control Systems (DeltaV).

Lead site compliance for biologics manufacturing: develop and maintain compliance programs, prepare for and host regulatory inspections, manage compliance team, track and mitigate quality risks, run self-inspections and KPIs, drive continuous improvement, manage audits and corrective actions, and maintain stakeholder/regulator relationships to ensure GMP and regulatory adherence.

Lead global training governance for Sanofi's R&D Global Training Center: manage LMS (iLearn) administration, ensure GxP-compliant training matrices and plans, drive KPIs and corrective actions, support audits, harmonize global practices, and guide SMEs on compliant training content and initiatives.

Support scouting, validating, and transitioning AI-enabled and digital regulatory capabilities from early discovery to business-as-usual. Analyze feasibility and value, coordinate handovers, track maturity and adoption metrics, and produce dashboards, documentation, and communications to scale initiatives within R&D and regulatory teams.

Provide high-level executive support to the Global Head of Strategy & Operations and five senior directors. Manage complex global calendars, prepare meeting briefings, coordinate international travel and events, process expenses, maintain team resources (SharePoint, org charts), and liaise with senior stakeholders and counterpart EAs. Handle confidential materials with discretion and proactively manage shifting priorities in a fast-paced, strategy-focused biopharma environment.

Lead and execute end-to-end pharmaceutical market research projects to inform brand strategy. Select vendors, manage budgets and timelines, apply quantitative and qualitative methods (including AI-enhanced approaches), synthesize insights, and present actionable recommendations. Partner cross-functionally with commercial teams, drive agency relationships, and mentor junior staff to support product launch and GTMC strategic priorities.

Lead the large-scale monoclonal antibody (mAbs) drug substance facility project from early enabling works through design, construction, commissioning, qualification and handover. Provide engineering and project leadership to meet cGMP, safety and regulatory standards, drive on-time/on-budget delivery, manage CapEx and COGS, oversee Engineering/Automation/Maintenance/C&Q, integrate the new facility into the brownfield site, and build staffing, training and ramp-up plans to achieve routine manufacturing.

Lead clinical supply chain activities for IMPs, defining strategy, overseeing study management, monitoring KPIs, coordinating stakeholders, mitigating risks, and driving process improvements to meet timelines, quality, and budget across global clinical trials.

Lead financial integration for external manufacturing (CMOs), driving budgeting, forecasting, month-end close, cost accounting, inventory optimization, KPI tracking, and financial modeling. Partner with supply chain, procurement, operations, and central finance to ensure accurate reporting, SOX compliance, and smooth transitions from M&A or R&D to commercial manufacturing.

Support divisional GMs and field teams by operationalizing strategy, managing budgets/resources, delivering analytics and insights, training field staff, and driving cross-functional initiatives. Role includes ~40% travel and focuses on account planning, performance analysis, and professional development activities across a hematologic oncology franchise.

Serve as US Privacy Counsel and Privacy Officer for Sanofi: advise on GDPR/HIPAA/CCPA and state privacy laws, conduct DPIAs, manage breach investigations/notifications, liaise with regulators, train business teams, maintain processing records, and support privacy implementation across product and AI initiatives.

Partner with brand, media, digital, and data teams to design and execute consumer and media analytics, measurement, and attribution for DTC campaigns. Translate complex analyses into actionable insights, build scalable analytics capabilities (segmentation, lookalikes, journey analytics), support model development and dashboards, and drive cross-functional delivery while ensuring governance, QA, and privacy-aligned outputs.

Lead and execute supplier contract audits to validate compliance, quantify financial impacts, and drive corrective actions. Analyze documentation, engage stakeholders, identify risk-based targeting and improvement opportunities, contribute to audit tools and processes, and support cross-functional projects and reporting.