Jobs at Sanofi

Support HSE fieldwork, compliance, environmental reporting, training, and documentation. Conduct ATEX compliance surveys, produce waste/energy/water/cooling reports, assist safety and process-safety initiatives, create a safety induction video, perform ISO14001:2026 gap assessments, and deliver at least one HSE improvement project.

Support the procurement team with vendor management, supplier evaluation, spend consolidation, sourcing research, report and dashboard preparation, meeting representation, and procurement administrative tasks.

Participate in routine cGMP manufacturing across Upstream, Downstream, or Central Manufacturing Services. Operate and monitor equipment and digital/automation systems, maintain documentation and audit readiness, support batch records, deviations and change control, and contribute to continuous improvement initiatives within a 12-hour rotating shift.

Provide Tier 3 multi-disciplinary project support, feasibility input, and third-party coordination; act as technical liaison between Manufacturing and Engineering for complex troubleshooting, commissioning, and process improvements; support system lifecycle, handovers, and root-cause investigations in a GxP biopharmaceutical manufacturing environment.

Lead Engineering & Maintenance compliance activities to ensure GMP/GxP inspection readiness. Manage deviations, CAPAs, change controls, audits, investigations, and continuous improvement. Collaborate with Quality, Validation, and Engineering to strengthen quality systems, review procedures, train staff, and support reliable biologics manufacturing operations.

The Associate Engineer supports upstream biopharmaceutical manufacturing operations by monitoring processes, ensuring compliance with GMP, and contributing to continuous improvement efforts.

Support automation engineers in manufacturing operations by collecting and analyzing process and alarm data, performing root-cause analysis, improving documentation (change controls, drawings), identifying critical spare parts, and assisting with daily team tasks and metric updates.

Lead site Tier-3 engineering and projects for the Tuas Modulus site: manage T3 capex (<5M€), feasibility/front-end studies, project execution (design, procurement, construction, C&Q), process engineering support, vendor/contract management, standards/compliance (GMP/FDA), and team staffing and development.

Lead and oversee internal and external communication strategies, manage corporate messaging, media relations, and stakeholder communications, ensuring alignment with global communication objectives and local market needs.

Serve as site SME for the plant historian platform (AspenTech IP.21), ensuring high availability, GMP compliance, data integrity and validated data connectivity with MES/DeltaV/SCADA. Lead CSV activities, troubleshoot and optimize system performance, support digital transformation, develop SOPs and validation documentation, manage vendors/spares, and represent the system during audits.

Lead and develop an upstream MSAT team to support process transfer, validation, manufacturing troubleshooting, and continuous improvement. Own upstream process platforms, drive technology implementation and CPV, manage projects and budgets, author regulatory technical documents, and provide after-hours manufacturing support and complex investigations to ensure robust large-scale mammalian bioprocessing.

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.

Support material release performance and data analysis, assist quality walkdowns and shop-floor oversight, collect and analyze production/QC quality data, monitor deviation/CAPA/change control metrics, and contribute to investigations and corrective actions.

Participate in commissioning, qualification, and operational readiness of a modular biomanufacturing facility. Execute routine cGMP upstream/downstream manufacturing activities, support tech transfers, documentation, audits, and continuous improvement. Use digital and automation systems (ERP/MES/PCS), and work rotating 12-hour shifts during validation and production.

The Senior Biotechnologist will oversee commissioning and qualification activities, conduct GMP manufacturing, and support regulatory readiness in a biopharmaceutical facility.

Lead deployment, governance and continuous evolution of the Sanofi Manufacturing System (SMS) at site level. Drive operational excellence, transformation initiatives, performance monitoring, benefits realization, capability building and SMS operating standards in a cGMP manufacturing environment, partnering with site leadership, global SMS teams and cross-functional stakeholders.

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.