Reference No. R2745824

Position Title: Manager Batch Production Records

Duration: Fixed-Term - Contract End Date: March 27, 2026

Department: Document Management

Location : Toronto, Ontario

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. Your job, as Production Manager within Product Quality, will be to ensure a consistent and efficient design by conforming to global quality directives, and regulatory and GMP requirements, while meeting needs of the shop floor staff. Lead and support continuous improvement initiatives and regulatory commitment projects such as, new product/process development and Business Continuity Plan. Provide support in troubleshooting and problem-solving system issues and connect with local support technical team or the vendor for support, as required and on a priority basis.

Vaccines

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:

• Create new Master Batch Production Records and revise existing ones as per area requests and change controls utilizing the management system.

• Act as a liaise with various stakeholders across site including Quality Operations, Manufacturing and Manufacturing Technology to facilitate the development and maintenance of production records.

• Manage priorities and meet critical timelines for both internal customers and regulatory agencies with moving priorities.

• Ensure inspection readiness of the area, mitigate risks, and provide inspection support.

• Assist in investigation of deviations related to system and department processes.

About you:

• Ability to work within critical timelines.

• Strong background in all stages of biological product manufacturing is an asset.

• Minimum 5 (five) years pharmaceutical cGMP or similar related certification and experience.

• Minimum Bachelor of Science or Engineering, or related field.

• Excellent written and verbal communication skills, report writing, strong attention to detail and exceptional organization skills

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 and at least 14 weeks’ gender-neutral parental leave.

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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