Job opportunity
Biopharmaceutical Manufacturing Technologist
Sanofi Group
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.
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Apply on source site 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.
#J-18808-Ljbffr