Technical Group Leader- Vaccines

BioTalent Canada; Toronto; On-site; CAD 80,000 - 110,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Technical Group Leader to coordinate operations and ensure compliance with GMP guidelines. This role requires a diploma in a relevant field and experience in pharmaceutical manufacturing. Join a supportive team to lead transformative projects that impact public health.

Benefits

Employee benefit programs

Qualifications

• Minimum of three years relevant work experience required.
• Experience with automated and manually operated process equipment is preferred.

Responsibilities

• Coordinate daily tasks of technical staff and verify documentation compliance.
• Oversee data management for Influenza manufacturing operations.
• Ensure GMP compliance and lead process improvement efforts.

Skills

pharmaceutical manufacturing

protein purification

data management systems

cGMP

Education

College Diploma in Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences

Bachelor’s degree in a related field

Job description

Join Sanofi’s pioneering B200 operations in Upstream 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:

• 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.
• 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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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.