Apply aseptic technique and cGMP expertise as a Technologist supporting Sanofi’s vaccine manufacturing operations in Toronto, Ontario.

This fixed-term, eight-month contract supports drug substance manufacturing across Media, Buffer, Washing, Sterilization, Inoculation, Upstream, and Downstream activities. The Technologist reviews records, executes production activities, supports validation, and maintains accurate documentation. Work includes SAP, LIMS, environmental monitoring, analytical testing, and technical staff guidance. The schedule includes Tuesday-Saturday, Sunday-Thursday, or Friday-Tuesday shifts from 2:00 PM to 10:00 PM, subject to change. Training runs Monday-Friday, 8:00 AM-4:00 PM, subject to change.

Key Responsibilities:

- Prepare media, buffers, inocula, and sterilization activities
- Review GMP records, SOPs, logbooks, and monitoring charts
- Execute and verify IQ, OQ,



PQ, and cleaning protocols
- Complete SAP, LIMS, PCS, and environmental monitoring documentation
- Support deviations, root cause analysis, CAPA, and process improvements

Requirements:

- Three-year college diploma plus 18 months relevant experience
- Or four-year bachelor’s degree plus one year relevant experience
- Education in life sciences, chemistry, or related disciplines
- Knowledge of cGMPs, aseptic technique, and purification processes
- Technical writing, mathematics, computer, quality, and safety skills

Support Sanofi Vaccines with aseptic processing, GMP documentation, validation, and drug substance manufacturing expertise in Toronto.

📌 Biopharmaceutical Manufacturing Technologist (Toronto)
🏢 Sanofi Group
📍 Toronto