Sanofi
pharmaceutical manufacturing
TechnicalGroupLeader-MWS
Neural analysis suggests this role is
optimal for Mid candidates.
“Technical Group Leader-MWS at Sanofi. Skills: Technical Group Leadership, Pharmaceutical Manufacturing Operations, GMP Compliance, Team Supervision, Process Improvement. Administration of Influenza manufacturing activities. Scheduling and coordinating daily/weekly work of technical staff”
What You'll Achieve.
ensure timely completion of production activities; ensure all data input is completed accurately and in a timely manner; ensure completion of utility sampling and environmental monitoring on schedule; manage CCR, CAPA in Quality system until completion as per committed due dates
Industry & Context.
lead investigations; problem solving; troubleshooting
Fixed-Term - Contract (24 months), Onboarding and training period requires Monday-Friday 8:00 AM-4:00 PM, followed by afternoon shift (Tuesday-Saturday 2 pm to 10 pm), Workday application form must be complete with resume attached
What They're Looking For.
Must Have
Minimum 3 years College Diploma in Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related Life Sciences field, Minimum of three (3) years of relevant work experience, or equivalent, Experience with both Automated and manually operated process equipment, understanding of Computerized systems, Data management systems, Quality management systems, SAP, SOPs, automation, and other relevant software/applications
Nice to Have
Bachelor’s degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related Life Sciences), Proficiency in pharmaceutical manufacturing, protein purification, centrifugation, tangential flow filtration, and cGMP
What You'll Do.
Administration of Influenza manufacturing activities
Scheduling and coordinating daily/weekly work of technical staff
Reviewing and ensuring accuracy of documentation (Records
Ensuring equipment is in good GMP condition
Managing inventory of chemicals
Training technical staff on GMP
Facilitating meetings and reporting findings
Initiating and managing deviations and investigations
Coordinating with internal and external departments
Supervising material handling
Overseeing SAP activities and data management
Capacity planning and scheduling
Maintaining master recipes and production inventory
Performing production calculations and release checks
Ensuring cleaning standards are met
Monitoring process deficiencies and equipment condition
Performing utility sampling and environmental monitoring
Ensuring area is inspection ready
Ensuring ergonomic operations and hazard escalation
Coordinating facility
and process improvement projects
Writing and modifying specifications
and PQ for new equipment
Initiating and managing CCR
How You'll Work.
Team & Collaboration
Collaborate with industry experts; Coordinate and support units within department (Upstream, Downstream, MWS); Coordinate and support other outside departments (Maintenance, Automation, QO test labs); Coordinate and schedule work with Manufacturing Technology (MTech) and facility management (Engineering & Technical Services)
Communication Scope
Facilitate daily meetings; report findings to management; escalate any potential hazards
Process & Methodology
leading investigations, managing deviations, managing CCR, CAPA, coordinating and scheduling work of technical staff in facility, equipment, and process improvement projects
Full Job Description
**R2856563 - Technical Group Leader-MWS** **Duration:** Fixed-Term - Contract (24 months) **Location:** Toronto, Ontario **About the job** 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. Join Sanofi's pioneering B200 operations in Downstream team as a Technical Group Leader, spearheading innovation in pharmaceutical manufacturing. Collaborate with industry experts to drive excellence in operations and lead transformative projects. This exciting opportunity offers a platform to make a tangible impact in the intersection of technology and healthcare. We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world. **About Sanofi** We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. 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. Together, we chase the miracles of science to improve people’s lives. ** _Main Responsibilities:_** **Administration of Influenza manufacturing activities.** * Schedule and coordinate daily/weekly work ofa group oftechnical staff in B200 as per area requirements. * Check and review Records, SOP, logbooks/e-logbooks, BPRs/e-BPRs, and monitoring charts for completion and accuracy of all documents as per GMP guidelines. * Ensure equipment is kept in good GMP condition (with preventive maintenance, validation and calibration) * Order and ensure a
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