B100 DT Downstream Manager- Vaccines

Location: Toronto, Ontario

Duration: Unlimited Fixed Term

About the Job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.

The B100 operations manager is responsible for the relevant manufacturing operations in compliance with cGMP according to their specific production area (upstream, downstream, MWS, etc).  The manager is responsible for the daily activities of unionized staff in a cGMP facility in compliance with company policies.  This includes responsibility for the scheduling and execution of all operations with adequate level of GMP documentation.  This includes support from a user perspective for B100 project activities and adherence to SOPs, cGMP and HSE procedures.

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:

• Manage B100 operations, review and approve technical documentation, and manage miscellaneous equipment.

• Develop and manage production schedules, preventative maintenance, and manufacturing recipes; support validation activities and ensure project timelines.

• Ensure GMP compliance, develop quality initiatives, maintain operating procedures, conduct inspections, and lead audits.

• Organize and develop staff, provide feedback, ensure training, and manage hiring and attendance.

• Implement lean management systems, troubleshoot manufacturing issues, and lead process efficiency initiatives.

• Ensure workplace safety, report incidents, provide protective equipment, and promote EHS awareness.

• Manage manufacturing documentation, support budget development, and communicate project milestones.

About You

• Minimum bachelor's degree in microbiology, Biochemistry, Engineering or a related science.

• 1-3 years of relevant experience in Commercial Manufacturing, Manufacturing Technology, preferred.

• Strong knowledge of cGMPs in pharmaceuticals/biological manufacturing and experience in regulatory inspections.

• Excellent problem-solving, communication, and organizational skills, with strong technical writing abilities.

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.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs

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.