Technical Group Leader- Vaccines

卡湯晩; Toronto; On-site; CAD 80,000 - 110,000; Full time

Job summary

A leading global healthcare company seeks a Technical Group Leader to oversee vaccine production operations in Toronto. This role involves coordinating technical staff, ensuring compliance with GMP guidelines, and driving process improvements. Ideal candidates will have a relevant diploma and experience in pharmaceutical manufacturing, looking to make a significant impact in healthcare innovation.

Benefits

Supportive team environment

Opportunities for career advancement

Qualifications

• Minimum three years of relevant work experience in pharmaceutical manufacturing.
• Strong understanding of GMP and quality management systems.
• Experience with automated process equipment.

Responsibilities

• Coordinate daily/weekly tasks of technical staff under GMP guidelines.
• Oversee data management for manufacturing operations in Downstream.
• Lead process improvement efforts and prepare trending reports.

Skills

Pharmaceutical manufacturing

Protein purification

Centrifugation

Tangential flow filtration

Data management

Education

College Diploma in Biochemistry or related field

Bachelor’s degree in Biochemistry or related field

Tools

SAP

Job description

R2807275- Technical Group Leader- Vaccines

Duration: Fixed-Term Contract End Date: October 2027

Location: Toronto, Ontario

Join Sanofi's pioneering B200 operations in Downstream 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 500million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people andpromote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact onmillions 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:

• College Diploma (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related) with a 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.

Hours Of Work:

• Inclusive from Sunday, Monday, Wednesday and Thursday 10:00 p.m. - 08:00 a.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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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!