Technical Group Leader

Sanofi; Toronto; On-site; CAD 72,000 - 83,000; Full time

Job summary

Sanofi in Toronto, Ontario, is seeking a Technical Group Leader for the B200 infl uenza manufacturing operations. The role leads a technical staff team, ensures GMP compliance, and coordinates with multiple departments to meet production timelines and maintenance programs.

The candidate will oversee data management, SAP activities, and process improvements while upholding HSE standards within a GMP environment.

Qualifications

• Minimum 3 years of relevant work experience in biochemistry, microbiology, or related field.
• Preferred bachelor’s degree with 3+ years of related experience.
• Experience with pharmaceutical manufacturing and GMP is preferred.

Responsibilities

• Administer influenza manufacturing activities.
• Schedule and coordinate daily/weekly work of technical staff in B200.
• Review records, SOPs, logbooks, BPRs and monitoring charts per GMP.
• Ensure equipment is maintained per GMP with preventive maintenance.
• Train staff on GMP, SOPs and HSE requirements.
• Coordinate with Upstream, Downstream, MWS and other departments to meet production timelines.

Skills

GMP compliance

Pharma manufacturing

Protein purification

Automation & SAP

Data management systems

Education

Bachelor's degree in Life Sciences

College diploma in Life Sciences

Tools

SAP

Automation software

Quality management systems software

Job description

About the job

R2870590 Technical Group Leader Duration: Fixed-Term - Contract (July 2027) Location: Toronto, Ontario

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 staff 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 elevate 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 Of Work:

Inclusive from Monday - Friday 2:00 pm to 10:00 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.

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.

Pay rate - $54.52 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. TheData Subject Rights Webformcan also be used torequest 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 #LI-SP #LI-Onsite

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! We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.

Discover more about us visiting www.sanofi.com or via our movie We are Sanofi Start a career that makes a difference. Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.

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 Applications received after the official close date will be reviewed on an individual basis. This position is for a current vacant role that is now open for applications.