Teams 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.