B100 MBWS Production Manager- Vaccines
多伦多, 加拿大 Fixed Term 发布于 Dec. 03, 2025 申请截止于 Dec. 20, 2025 Salary Range CAD 76,200.00 - 110,066.66R2825797 B100 MBWS Production Manager- Vaccines
Location: Toronto, ON
Duration- 36 months
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 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.
R2825797 B100 MBWS Production Manager- Vaccines
Department: B100 MBWS
Location: Toronto, ON
Grade: L2
Duration: 36 months
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 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:
Support process design, startup, and troubleshooting across all project stages; review technical documentation; provide problem-solving guidance for manufacturing issues and implement corrective actions.
Develop and execute production schedules; lead shop floor operations teams; monitor performance metrics; support budget development; and establish effective communication protocols to meet project milestones.
Ensure GMP compliance in collaboration with quality teams; maintain current operating procedures and documentation; oversee shop floor compliance; and support regulatory audits and inspections.
Build high-performing teams through coaching and feedback; collaborate with B100 Operations management; manage hiring, onboarding, and performance of up to 20 unionized staff across shifts.
Implement lean management systems; lead efficiency and quality improvement initiatives; manage change control processes; and provide operational metrics and reports including PM plans and BOMs.
Ensure workplace safety compliance; promptly address health and safety concerns; identify hazards and enforce protective equipment usage; and collaborate with EHS management and Joint Health and Safety Committee.
Work effectively with QOOQ, QOSA, and other departments to achieve consensus on operational goals, project milestones, and quality initiatives while maintaining cGMP compliance.
Provide operational expertise throughout project lifecycle from URS development through engineering runs to full-scale manufacturing, ensuring seamless transition between project phases.
Scope and Dimensions:
Shift size : up to 20 Union staff
Oversees specific area of operations in Building 100
Develop and Ensure consistency of communication across shift
About You
Bachelor's degree in engineering or science.
Minimum 6 months of manufacturing experiencein a regulated environment (pharmaceutical, biotech, or related industry)
Ability to lead and coordinate teams in a manufacturing setting with strong communication, interpersonal, and cross-functional collaboration capabilities.
Knowledge of manufacturing processes, equipment operations, technical documentation (SOPs, batch records), and basic troubleshooting/problem-solving skills is preferred.
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
This position is for a new 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.
Toute compensation sera déterminée en fonction de l'expérience démontrée. 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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进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
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我们的产品设计师负责帮助人们提高免疫力,物流专家负责将药物送到需要的人手中,而数据分析师则借助先进的技术改善人们的生活。在医疗健康领域,每一次进步都离不开所有人的努力。您可以自由选择自己的职业发展道路。Gig零工项目将帮助您尝试更多岗位,个性化指导将为您挖掘自己从未被发现的优势。加入我们,开启菲凡的职业发展之路。您到底可以走多远?让我们拭目以待!
体验可能性
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Sustainable and Green
Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.
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我们的办公地点
我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。
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勇敢追梦,奔赴美好未来
想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。
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您和我们相互依存,共同成长
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心怀梦想,成就一番事业
我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。
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我们的人与文化
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我们的故事
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