Manager, Operational Quality - Vaccines

Reference No. R2758836

Position Title : Manager, Operational Quality - Vaccines (Open)

Location : Toronto, Ontario

Posting Date : Thursday, August 22, 2024

Closing Date : Monday, September 30, 2024.

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 Operation Quality Manager within our Quality team is to provide compliance support to Deputy Directors for the licensed product, teams in managing their day-to-day operations in compliance with Sanofi Pasteur quality systems requirements and Good Manufacturing Practices.

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 :

Support the Operational Quality Deputy Directors in ensuring timely review, follow-up on closure and approval of various documents, such as : master batch records, operational log books, SOPs, SWIs, deviations, protocols, reports, work orders, that are within the scope or delegated.

Project team participation.

Perform the role of QO Representative in coordinating, investigating and assessing Change Control Requests (CCR’s) and CAPAa as designated within this process.

This activity will require the incumbent to determine if a change request impacts product and processes.

In conjunction with the QO Quality System Internal Auditor and Vendor Auditor, perform audits and support functions performing GMP activities to ensure compliance with cGMP standards, site and corporate policies.

About you

Master of Science degree in Microbiology, Biochemistry or Immunology with 3+ years of relevant experience in Quality Operations from a Pharmaceutical or Biologics Manufacturing facility.

Act for Change, Cooperate Transversally, Strive for Results, Thinking Strategically.

Bachelor of Science degree specializing in Microbiology, Biochemistry, Immunology or Pharmacology with 5+ years of relevant experience in Quality Operations from a Pharmaceutical or Biologics Manufacturing facility.

Strong decision making 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.

GD-SP

LI-SP

LI-Onsite

Pursue , discover

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people people from different backgrounds, in different locations, doing different roles, all united by one thing : a desire to make miracles happen.

So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our and check out our Diversity Equity and Inclusion actions at !