Technical Group Leader- Vaccines

BioTalent Canada; Toronto; On-site; CAD 85,000 - 110,000; Full time

Job summary

A global healthcare company seeks a Technical Group Leader in Toronto to spearhead innovation in pharmaceutical manufacturing. The role involves coordinating technical staff and ensuring compliance with GMP guidelines. Candidates should have a strong background in biochemistry or related fields, along with experience in pharmaceutical processes and data management systems.

Benefits

Employee benefit programs

Diversity and inclusion initiatives

Qualifications

• Minimum of three years relevant work experience.
• Proficiency in pharmaceutical manufacturing processes.
• Strong understanding of computerized systems and data management.

Responsibilities

• Coordinate schedules for technical staff and ensure document accuracy.
• Oversee data management for Influenza manufacturing.
• Lead process improvement efforts and maintain safety standards.

Skills

Pharmaceutical manufacturing

Protein purification

Centrifugation

Tangential flow filtration

Data management systems

Quality management systems

SAP

SOPs

Automation

Education

College Diploma in Biochemistry or related

Bachelor’s degree in Biochemistry or related (preferred)

Tools

Automated process equipment

Manual process equipment

Job description

Join Sanofi’s pioneering B200 operations in MWS 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.

Main Responsibilities:

• Coordinate and schedule the daily and weekly tasks of the technical staff, while also reviewing and verifying the completion and accuracy of all documents, including Records, SOPs, logbooks/e-logbooks, BPRs/e-BPRs, and monitoring charts, in compliance with GMP guidelines.
• Coordinate and support units within department (Downstream) and other outside departments (Maintenance, Automation, QO test labs, etc.) and ensure timely completion of production activities.
• Oversee data management for Influenza manufacturing operations in Downstream and supervise the administration of related manufacturing activities.
• Ensure Health, Safety, and GMP environment maintenance; lead process improvement efforts and prepare trending reports.
• Coordinate technical staff’s schedules for facility, equipment, and process improvement projects with MTech and Engineering & Technical Services.

About You:

• Minimum 3 years College Diploma in Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related.
• 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) preferred, 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.
• Inclusive from Sunday-Thursday 2:00 p.m. – 10:00 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.

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 we are actively hiring for.

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.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Join Sanofi and step into a new era of science – where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch ‘One day at Sanofi’ and check out our Diversity Equity and Inclusion initiatives at sanofi.com