Jobs at Sanofi

Lead global strategy, development, and deployment of AI-ready data governance products and platforms. Own product lifecycle, standards, metadata, lineage, and data quality; ensure regulatory compliance, drive cross-functional adoption, and build high-performing teams to enable trusted enterprise data for business and R&D use.

As an AWS Cloud Engineer, you will design and build cloud foundations, develop infrastructure-as-code using Terraform, and automate deployments. You'll also ensure security and compliance and support cloud migration initiatives, acting as a technical advisor across teams.

As Product Design Lead, you will standardize user-centered digital experiences, drive Design System strategy, and collaborate with product teams to enhance product usability and design excellence.

The B100 APU Head manages a team ensuring vaccine manufacturing performance, quality, compliance, and innovation while fostering a collaborative culture.

Own global category strategy for Software, IT Services, and Hardware. Lead strategic negotiations and supplier relationships, deliver year-over-year savings, build sub-category roadmaps, manage risk and supplier scorecards, engage senior stakeholders and country procurement heads, and coach global procurement team while supporting Sanofi's AI-powered procurement transformation.

The Solution Architect will design enterprise solutions for global functions, lead digital transformation, collaborate with cross-functional teams, and manage architectural decisions aligned with strategic roadmaps.

The Statistical Project Leader oversees statistical contributions to clinical studies, ensuring quality and compliance, while mentoring team members and collaborating across functions.

Support External Workforce HR operations for master data and employee lifecycle activities, process tickets/queries (Workday, Fieldglass, VMS), coordinate offboarding, maintain documentation and KPIs, ensure GDPR compliance, drive continuous improvement, and act as a key contact for external workforce stakeholders.

Lead and coordinate global regulatory strategy and continuous-improvement initiatives across GRA CMC and GRA Device. Build cross-functional governance, track KPIs, resolve project dependencies, harmonize processes, validate CMC post-approval databases, support inspection-readiness, and drive tools/systems optimization and knowledge sharing across teams.

Lead scientific programming for vaccine clinical projects, manage programming deliverables and resources, ensure CDISC compliance and regulatory submissions, oversee CRO outsourcing, drive process improvements and automation, collaborate with statisticians, and mentor junior programmers.

Design, develop, and execute analytical methods (HPLC/UPLC, LC-MS, cIEF, binding assays) to support biologics R&D. Independently run non‑GMP testing, analyze and interpret data, draft technical reports, and drive project timelines while leveraging digital/AI tools and collaborating cross-functionally.

The Reliability and Methods Engineer enhances reliability and maintenance of GMP systems, develops strategies, audits compliance, supports maintenance planning and leads improvement actions.

Oversee daily operations of the QC lab, ensure regulatory compliance, manage staff training, and conduct investigations related to microbiological testing.

The QC Manager for Microbiology will lead daily operations of the microbiology team, ensuring compliance with cGMP standards, drive microbiological testing, address OOS results, collaborate cross-functionally, and promote operational excellence.

Assist HSE team implementing corporate initiatives and improvement projects for a new modular vaccine/biologics facility. Support site inspections, documentation and site programs, perform data analysis, and create digital promotional videos and online quizzes. Participate in general HSE tasks as needed.

The Supervisor, Manufacturing leads the startup and operations in bioprocess manufacturing, ensuring compliance, team management, and continuous improvements.

The Batch Release Lead investigates batch release issues, monitors quality metrics, leads root cause analysis, ensures compliance with regulations, and oversees documentation review.

Apply statistical and data-science methods (ML, NLP, forecasting) to optimize injectable manufacturing and tech transfer. Perform data analysis, AKM modelling, support Digital Twin/process modelling, deploy statistical best practices, develop site statistical systems, and provide oversight and training across the injectables network.

The Quality Control Analyst II will perform microbiological tests, conduct environmental monitoring, write QC documents, and maintain records in compliance with GMP standards.

Serve as single point of contact for GenMed China analytics, partnering with GBU/BU heads to deliver customer, market, and performance insights. Lead predictive analytics, forecasting, dashboards, scenario planning, and ROI analysis to support strategic planning, launches, and resource prioritization. Coordinate cross-functionally, translate data into executive presentations, and advise on China-specific market drivers (NRDL, VBP, DRG/DIP).