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Added 11 mins ago
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Non-Technical Publications Manager
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- Full-time
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Added 1 hour ago
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Added 1 hour ago
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Database Administrator
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Database Administrator
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Added 1 hour ago
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Sanofi

Technical Group Leader

Toronto, ON, Canada

Pay rate - $56.02 per hour. · Full-time

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Job details

Pay: Pay rate - $56.02 per hour.
Job type: Full-time
Apply by: Nov 5, 2026
Posting language: English
Posted: Oct 29, 2026

Original job description

Reference no. R2876619

Position title: Technical Group Leader

Duration: Fixed-Term - Contract (8 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 Upstream 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 of a group of technical 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 adequate chemicals, supplies, 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 (Upstream, Downstream, MWS) and other outside departments (Maintenance, Automation, QO test labs, etc.) and ensure timely completion of production activities.
Perform other duties as assigned by Department Management throughout all stages of drug substance manufacturing
Supervise material handling in B200 Shipping, Receiving, and storage areas.

Administration of Data for Influenza manufacturing.

Coordinate, oversee, 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 such as investigation data, LIMs, deviation filing, change request forms, etc.
Perform activities in PCS and review data as required

Perform area specific activities, monitoring, maintenance.

Perform and delegate production calculations, measurements and release checks. Ensure each cleaning meets standards set in SOP, records, 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 as required and ensure completion on schedule
Train technical staff on problem solving and troubleshooting as required.
Ensure area is inspection ready. Knowledgeable to guide inspectors

Oversight of Health, Safety, and maintenance of GMP environment.

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.

Process improvement, development and preparation of trending reports.

Coordinate and schedule work of technical staff in facility, equipment, and process improvement projects with Manufacturing Technology (MTech) and facility management (Engineering & Technical Services)
Write or modify specifications, protocols and reports related to facility, equipment, including SOP's, BPR's.
Perform activities involved in IQ, OQ, and PQ for new equipment
Initiate CCR, CAPA in Quality system as needed and manage them until completion as per committed due dates

About You

Experience / Skills / Qualifications:

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.
Preferred Bachelor’s degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related Life Sciences), with a minimum of three (3) years of relevant work experience.
Proficiency in pharmaceutical manufacturing, protein purification, centrifugation, tangential flow filtration, and cGMP preferred.
Experience with both Automated and manually operated process equipment.
Strong understanding of Computerized systems, Data management systems, Quality management systems, SAP, SOPs, automation, and other relevant software/applications.

Hours/Shift Of Work:

Friday to Tuesday from 06:00 a.m. - 02:00 p.m. (Subject to change)

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.

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.
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-crafted rewards package that recognizes your contribution and amplifies your impact.

Mandatory Application Requirement: Your Workday application form must be complete, and a copy of your resume MUST be attached in the Workday application form, at the time you submit your Workday application, otherwise your application will not be considered for this position

This position is for a current vacant role that is now open for applications.

Pay rate - $56.02 per hour.

AI Usage

"Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company’s Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal,  Data Subject Rights Webform. The Data Subject Rights Webform can also be used to request access or correction of your personal information and file a complaint.

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request.

#GD-SP

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

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More about this job

Responsibilities

The Technical Group Leader will oversee daily influenza manufacturing activities, ensuring compliance with GMP guidelines and coordinating technical staff schedules. They are responsible for managing production data, leading investigations into deviations, and facilitating process improvements within the manufacturing unit.

Requirements

Candidates must possess at least a 3-year College Diploma in a relevant Life Sciences field and a minimum of three years of work experience. Proficiency in pharmaceutical manufacturing processes, cGMP, and computerized systems like SAP is required.

Skills

Pharmaceutical manufacturing
GMP
SOP
SAP
Data management
Quality management systems
Protein purification
Centrifugation
Tangential flow filtration
Automation
Team leadership
Deviation investigation
Capacity planning
HSE compliance
Technical documentation
Equipment maintenance

Benefits

Rewards package

Visa sponsorship

Not detected in the job text

Keywords

Biopharma
Manufacturing
Influenza
GMP
SOP
SAP
Biochemistry
Microbiology
Bioengineering
Biotechnology
Chemistry
Chemical Engineering
Pharmaceutical Sciences
Protein purification
Centrifugation
Tangential flow filtration
cGMP
Automation
Data management
Quality management
HSE
PPE
IQ
OQ
PQ
CAPA
CCR
LIMS
BPR
Upstream

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