B200 Operations Manager (Media, Washing and Sterilizing)- Vaccines - #450820
Sanofi
Date: 5 hours ago
City: Toronto, ON
Salary:
CA$76,200
-
CA$110,066.66
per year
Contract type: Full time

R2807483 B200 Operations Manager (Media, Washing and Sterilizing)- Vaccines
Department: B200 Operations – Buffers, MWS & Logistics
Duration: Fixed Term Contract, 18 months
Location: Toronto, Ontario
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 B200 MWS Manager is responsible for manufacturing operations in the Buffer Preparation, Washing & Sterilizing, and Raw Materials areas of Building 200. The manager is responsible for the daily acitivities 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 also includes active involvement in B200 project activities, from design to commercial operations.
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
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
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.
Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise. Des informations supplémentaires sur les avantages sociaux peuvent être trouvées ici.
Department: B200 Operations – Buffers, MWS & Logistics
Duration: Fixed Term Contract, 18 months
Location: Toronto, Ontario
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 B200 MWS Manager is responsible for manufacturing operations in the Buffer Preparation, Washing & Sterilizing, and Raw Materials areas of Building 200. The manager is responsible for the daily acitivities 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 also includes active involvement in B200 project activities, from design to commercial operations.
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
- Lead MWS processes and equipment operations through Development and PPQ through to Commercial Operation.
- Develop and execute production schedules from project through full-scale manufacturing, ensuring timely delivery of project milestones and deliverables.
- Ensure cGMP compliance and quality standards, develop continuous improvement initiatives, and support internal/external regulatory audits and inspections.
- Author/Review/Approve technical documentation, work instructions, and SOPs.
- Review and approve technical documentation (P&ID, IOQ, PPQ, design documents) and manage procurement of small equipment for engineering runs.
- Implement lean management systems and lead continuous improvement initiatives to increase process efficiency, quality, and yield.
- Provide troubleshooting and problem-solving guidance for daily manufacturing issues and implement preventative/corrective actions.
- Ensure workplace safety compliance including HSE policies, HAZOP understanding, safety training, and incident reporting protocols
- Bachelor's degree in microbiology, Biochemistry, Engineering, or Related Sciences required
- Minimum 2-5 years pharmaceutical industry/manufacturing experience.
- People management experience preferred
- Experience with manufacturing automation (e.g., DeltaV) and electronic batch records preferred
- Business/management training considered an asset
- 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.
#GD-SP
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.
Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise. Des informations supplémentaires sur les avantages sociaux peuvent être trouvées ici.
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