Jobs at Sanofi

Leads the establishment and operation of Sanofi’s Asia Regional Treasury Center in Singapore. Oversees treasury processes, staffing, cash and liquidity management, working capital optimization, forecasting, foreign exchange exposure, trade finance, banking relationships, intercompany activities, compliance, controls, and treasury technology. Partners with corporate, regional, local, banking, tax, legal, and finance stakeholders while managing teams, driving process standardization, supporting strategic projects, and ensuring operational excellence across Asian markets.

Performs commissioning, qualification, technology transfer, and GMP manufacturing activities for biopharmaceutical production. Supports engineering and product validation runs, equipment and system readiness, training, regulatory and audit preparation, deviation investigations, continuous improvement, and digital manufacturing operations. Works in upstream, downstream, or central manufacturing services on a rotating twelve-hour day and night shift, including weekends when operational.

Manage daily pharmaceutical Quality Control laboratory operations, ensuring GMP compliance, accurate testing, method validation, equipment qualification, staff training, investigations, deviations, CAPAs, and audit readiness. Lead and develop laboratory personnel, review analytical results supporting batch release, maintain laboratory facilities and instruments, and drive quality, safety, operational excellence, and continuous improvement.

Performs routine cGMP manufacturing operations across upstream, downstream, or central manufacturing services. Operates and monitors equipment, digital automation systems, and manufacturing software; maintains documentation, audit readiness, housekeeping, batch records, deviations, and change controls. Supports continuous improvement and process optimization while working on a 12-hour rotating day and night shift schedule.

Manages pharmaceutical quality operations, including batch record review, batch disposition and release, deviations, laboratory investigations, CAPAs, change controls, and qualification and validation documentation. Leads root-cause investigations, audits, regulatory inspection support, risk management, and continuous improvement initiatives while ensuring compliance with GMP, FDA, EMA, and company quality standards. Partners with manufacturing, validation, and cross-functional teams to resolve shop-floor issues and maintain product quality.

Owns the site Manufacturing Execution System, including configuration, architecture, integrations, maintenance, validation, compliance, troubleshooting, upgrades, and continuous improvement. Serves as the MES business system owner and technical subject matter expert, supporting manufacturing operations, site projects, audits, inspections, cybersecurity, data integrity, vendor management, documentation, training, and system reliability.

Performs microbiological, bioburden, and endotoxin testing of water, raw materials, and product samples in a GMP-regulated pharmaceutical facility. Conducts environmental and water monitoring, aseptic sample dispensing, incubation, observations, and result documentation. Develops QC SOPs and risk assessments, maintains data integrity, and supports continuous improvement. The role contributes to establishing and operating a new microbiology QC laboratory at Sanofi’s Singapore Modulus facility.

Provides pharmaceutical Quality Assurance oversight for final drug substance disposition, batch release, deviations, change controls, Product Quality Reviews, investigations, audits, and regulatory inspections. Ensures compliance with GMP and quality systems, leads root cause analysis, evaluates product quality impacts, supports corrective and preventive actions, and drives continuous improvement through metrics and trend analysis. Partners cross-functionally with Manufacturing, Quality, Regulatory, and site stakeholders.

Provides technical expertise for upstream and downstream biopharmaceutical manufacturing processes during facility startup and routine operations. Supports commissioning, qualification, validation, DeltaV and MES workflow development, equipment troubleshooting, investigations, deviations, CAPA, change controls, and continuous improvement. Serves as a process subject matter expert and leads cross-functional efforts to improve equipment reliability, manufacturing performance, and cost effectiveness.

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

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.

As a Quality Control Analyst I, perform microbiological testing, environmental monitoring, and maintain GMP-compliant records at a new QC laboratory.

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

Support site Quality Systems and Compliance by assisting QMS implementation, digital documentation (electronic logbooks/forms), document archival/destruction, Quality Culture and Data Integrity programs, tracking quality gaps/actions and site quality projects, and supporting inspection readiness logistics.

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 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.

Own and optimize biopharmaceutical manufacturing processes and equipment, including media and buffer preparation, autoclaves, column packing, and automated logistics. Lead continuous improvement, change controls, reliability initiatives, risk assessments, deviations, root-cause investigations, CAPAs, qualification, validation, and GMP compliance. Collaborate with Manufacturing, Quality, MSAT, Automation, engineering teams, and vendors to improve process robustness, efficiency, and operational reliability while supporting NPI and startup activities.

Supports corporate communications and public affairs through campaign ideation, writing and editing, event coordination, stakeholder engagement, advocacy initiatives, political monitoring, documentation compliance, and regional communications support. The intern will develop communications, project management, stakeholder mapping, ethical lobbying, and brand management skills within a pharmaceutical environment.

The Specialist II will provide Quality oversight for GMP operations, ensure compliance with global standards, support digital initiatives, and lead quality improvements during manufacturing operations.

Plans and maintains pharmaceutical production schedules based on supply plans, qualification, and maintenance activities. Monitors progress, adjusts schedules for delays, performs scenario planning and capacity modeling, coordinates material availability and finished-product delivery, analyzes bottlenecks, improves efficiency, and maintains production documentation. Collaborates with production, supply chain, engineering, and maintenance teams.