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Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

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Sanofi Group Quality Manager (Supplier) - Vaccines in Toronto, Ontario

Reference No. R2743022

Position Title: Quality Manager (Supplier) - Vaccines

Department: B100 Operational Readiness

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. Your job, as a Manager, Quality & Operational Readiness within our building 100 Operational Readiness, will be to involve in managing supplier change notifications, deviations, specifications, and change controls while fostering professional relationships and upholding Regulatory and Sanofi quality standards.​

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:

  • Negotiate and Establish Quality and Technical Agreements with Third Parties, and other Sanofi entities for products, materials, and Services.

  • Ensure quality oversight on all managed materials and services, including specifications and assessments.

  • KPIs related to Third-Party complaints and compliance management.

  • Ensure alignment to cGMP, regulatory and internal requirements.

  • Works independently under minimal supervision and direction to complete planned activities e.g., determine adequacy of investigations performed by suppliers and service providers.

About you

  • Strong technical writing and communication skills.

  • Competencies include technical writing, international GxP knowledge, and customer commitment.

  • Experience in GMP pharmaceutical/biological manufacturing, electronic database management

  • Bachelor of Science Degree in Chemistry, Biochemistry, or related field.

  • Act for Change, Cooperate Transversally, Strive for Results, Commit to Customers.

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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