Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster. Sanofi’s global vaccines business unit partners with the public health, medical and scientific communities to improve access to life-protecting vaccines and increase vaccination coverage, while striving to develop new and improved vaccines to enhance health and well‑being. We believe our cutting‑edge science and manufacturing, fueled by data and digital technologies, have the potential to transform the practice of medicine, turning the impossible into possible for millions of people. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Assist in review of Records, SOP, logbooks, and monitoring charts for completion and ensure accuracy of all documents as per GMP guidelines. Train and ensure technical staff comply to GMP, HSE, and SOP requirements. Participate in deviation investigations and root cause analysis. Coordinate with units within department (MWS, Upstream and Downstream) Provide training to personnel. Execute and verify IQ/OQ/PQ validation and cleaning verification protocols. Perform other duties as assigned by department management throughout all stages of drug substance manufacturing related to (MWS, Upstream and Downstream processes). Preparation of media, buffer, washing and sterilization, inoculum, analytical testing, area monitoring, maintenance, material handling, warehouse Perform activities and documentation involved in MBWS and Upstream including, in buffer preparation, washing and sterilizing, inoculation preparation, infectivity testing,



and material handling. Perform production calculations, measurements, and release checks. Observe in detail and report any process deficiencies, perform visual inspection of equipment for impurity and damage before and after cleaning. Perform utility sampling and environmental monitoring as required and ensure the completion as adhered to schedule. Provide guidance to technical staff on problem solving and trouble shooting. Ensure area is inspection ready. Material handling, movement an organization and storage. Administration of data for drug substance operations and preparation of trending reports for analysis Document and review production and monitoring activities for drug substance manufacturing Complete SAP transactions in a timely, accurate manner. Draft, review and revise cGMP documents (SOPs/SWis, batch records, protocols, change controls, reports and other manufacturing supporting documents). Ensure all data is completed timely and accurately in LIMS, Master, Change Request Forms, PCS and EM svstem. Participate in keeping the production area and office areas in a tidy, GMP manner, following 5S guideline or equivalent and supply materials as required Assist to ensure loading dock and hallways are clean and unobstructed by materials or equipment, garbage is discarded daily to designated area outside production. Follow HSE SOP’s, identify and minimize risks, promote safety culture.



Ensure chemicals are stored as per HSE requirement and has MSDS available. Process improvement and development Assist implementation of facility, equipment, and process improvement projects. Assist in writing specifications, protocols and reports related to facility, equipment, and process improvement of production process. Modification of SOPs and BPR’s for current processes in accordance with change control policies. Initiate Deviations, CCR, CAPA in Quality system as needed and assist until completion as per committed due dates. Collaborate with other departments for root cause analysis and assist with implementation of corrective actions. Minimum (3) three years College Diploma or equivalent (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science, (or equivalent education) plus a minimum of one (1) year and six (6) months of previous relevant work experience. 4) four years Bachelor’s degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science, or equivalent) plus a minimum of (1) one year of previous relevant work experience. Functional, Technical or scientific Production Equipment. Current Good Manufacturing Practices (cGMPs). Mathematics, Computer, Mechanical Aptitude, Technical Writing, Quality and Improvement, Safety. Supervisory, Managerial and Personal Communication I Networking Inclusive from Sunday to Friday, 10 pm to 6 am. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well‑cra

📌 Technologist (Night Shift) (Canada)
🏢 BioTalent Canada
📍 Canada