Jobs at Sanofi

Design, implement, operate, and maintain BMS and EMS automation systems for regulated pharmaceutical manufacturing facilities. Manage automation projects from specification and design through commissioning, qualification, start-up, and handover. Ensure cGMP, GAMP, CSV, data integrity, cybersecurity, and regulatory compliance. Support HVAC and utility automation, FAT/SAT, troubleshooting, root-cause investigations, CAPA, continuous improvement, vendor management, procurement, documentation, audits, and technical training.

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.

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.

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.

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.

Conducts risk-based internal audits of Asia Pacific pharmaceutical operations, including risk assessments, fieldwork, control testing, evidence collection, deficiency analysis, and audit reporting. Communicates findings and recommendations to stakeholders, promotes internal-control best practices, maintains audit documentation and quality standards, supports audit planning and methodology development, and participates in internal audit work groups and training.

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.

Supports commissioning and qualification of biomanufacturing equipment and digital systems, executes GMP manufacturing and validation runs, maintains manufacturing areas, assists with regulatory documentation and audits, and contributes to tech transfer and continuous improvement. The role involves hands-on biologics manufacturing across upstream, downstream, or central manufacturing services teams, with potential day or rotating shift work at the Tuas facility in Singapore.

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.

Perform and oversee GMP environmental monitoring, including sampling, data review, trending, scheduling, and documentation. Lead equipment qualification, calibration, investigations, CAPAs, change controls, SOP ownership, validation support, and microbial isolate management. Serve as the Environmental Monitoring SME and trainer while supporting QC microbiology testing and cross-functional collaboration with Manufacturing, Engineering, Validation, and QA teams at a new vaccine and biologics manufacturing facility.

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.

Serves as the local QC digital systems expert, deploying and maintaining LabWare LIMS and other GxP laboratory systems. Manages validation, master data, user access, equipment qualification, calibration, maintenance, investigations, CAPAs, change controls, and regulatory documentation. Supports audits and inspections, trains end users, ensures data integrity and cGMP compliance, and leads continuous improvement for QC laboratory systems and equipment.

Supports pharmaceutical equipment requalification, GMP compliance, SOP updates, document control, audits, deviation investigations, CAPA implementation, facility reviews, and pest-control assessments. Coordinates with Engineering, Production, Validation, and vendors; maintains schedules and documentation to support regulatory compliance and audit readiness.