Sanofi
pharmaceutical manufacturing
TechnicalGroupLeader-MWS
Neural analysis suggests this role is
optimal for Mid candidates.
“Technical Group Leader-MWS at Sanofi. Skills: Administration of Influenza manufacturing activities, Administration of Data for Influenza manufacturing, Perform area specific activities, monitoring, maintenance, Oversight of Health, Safety, and maintenance of GMP environment, Process improvement, development and preparation of trending reports. Schedule and coordinate daily/weekly work of a group of technical staff. Check and review Records, SOP, logbooks/e-logbooks, BPRs/e-BPRs, and monitoring c”
What You'll Achieve.
ensure timely completion of production activities; ensure all data input is completed accurately and in a timely manner; ensure completion on schedule; Ensure area is inspection ready; manage them until completion as per committed due dates
Industry & Context.
Train technical staff on problem solving and troubleshooting
Fixed-Term - Contract (24 months), During the period of onboarding and training (approximately 6 months) you will be required to work 5 days a week, Monday through Friday 8:00 AM- 4:00 PM and then you will be moved to afternoon shift i. e. , Tuesday through Saturday 2 pm to 10 pm. This is subject to change at any time, and it should not be construed as limiting the right of the company to make such change to meet the requirements of the operation.
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.
Schedule and coordinate daily/weekly work of a group of technical staff
Check and review Records
and monitoring charts for completion and accuracy
Ensure equipment is kept in good GMP condition (with preventive maintenance
validation and calibration)
Order and ensure adequate chemicals
and spare parts for equipment
Train and ensure technical staff comply to GMP and SOP requirements
Facilitate daily meetings and report findings to management
Initiate and file deviations and lead investigations
Coordinate and support units within department and other outside departments
Supervise material handling in Shipping
and confirm technical staffs completion of SAP activities/transactions
Capacity planning and scheduling of materials and personnel
Create work orders for ETS/Maintenance
Maintain master recipes and production inventory
Create and maintain process orders with authorization to change orders upon demand
Ensure all data input is completed accurately and in a timely manner
Perform activities in PCS and review data as required
Perform and delegate production calculations
measurements and release checks
Ensure each cleaning meets standards set in SOP
and in accordance with GMP
Observe in detail and report any process deficiencies
Perform visual inspection of equipment for impurity and damage before and after cleaning
Perform and delegate utility sampling and environmental monitoring
Train technical staff on problem solving and troubleshooting
Ensure area is inspection ready
Train and ensure technical staff comply with HSE requirements
Ensure operators are equipped and use proper PPE when performing tasks
Ensure operations are performed in an ergonomic way and escalate any potential hazards
Help develop proposed solutions
Ensure routine HSE checks and inspections are completed in a timely manner
Ensure cleaning chemicals and equipment are stored and used as per HSE requirements and have SDS available
Coordinate and schedule work of technical staff in facility
and process improvement projects
Write or modify specifications
protocols and reports related to facility
Perform activities involved in IQ
and PQ for new equipment
CAPA in Quality system as needed and manage them until completion
How You'll Work.
Team & Collaboration
Collaborate with industry experts; Coordinate and support units within department (Upstream, Downstream, MWS) and other outside departments (Maintenance, Automation, QO test labs, etc.); Coordinate and schedule work of technical staff in facility, equipment, and process improvement projects with Manufacturing Technology (MTech) and facility management (Engineering & Technical Services)
Communication Scope
Facilitate daily meetings; report findings to management
Process & Methodology
lead investigations, manage CAPA until completion
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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