Analytical Scientist
Toronto, Canada Permanent Posted on Mar. 24, 2025 Closing on Apr. 18, 2025Reference No. R2785498
Position Title: Analytical Scientist- Vaccines
Department: References & Critical Reagents
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.
The Analytical Scientist in QC Analytical Excellence References and Critical Reagents team is responsible for providing technical guidance for activities related to the qualification and use of reference standards and critical reagents for QC assays. The incumbent is responsible for managing quarterly trending of QC RCRs, requesting materials, expiry date extensions, write protocols and reports, lead RCR qualifications and collaborate with Biostats for statistical analysis, and timely implementation of replacements. The incumbent will liaise with internal and external stakeholders for dispatches, initiate and manage change controls. This role includes supporting troubleshooting/investigational activities, analytical projects, regulatory audits, and continuous improvement initiatives.
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:
Manage activities related to qualification of references and critical reagents in QC labs. Work with cross-functional teams to ensure timely material requests, qualification, and implementation. Collaborate with Biostats for statistical analysis.
Initiate and manage change controls.
Author protocols and reports for qualifications of references and critical reagents.
Audit trend data for QC references and critical reagents to monitor performance.
Provide support in analytical projects, such as new test method implementations in QC.
Manage dispatches between QC labs, Sample Management, HSE, Toronto Export group and Shipping department to ensure reagents are shipped in accordance with internal and external policies/regulations. Liaise with external stakeholders on inquiries related to references and critical reagents.
Manage expiry extensions by performing data analysis and preparing reports.
Support budgeting activities to align team activities with cross-functional teams on site. Delegate tasks as appropriate and develop indirect reports.
Support regulatory audits, global continuous improvement initiatives, and site strategic projects.
About You
Key Requirements:
BSc degree in Life Science or a related disciplines and at least three years of experience or MSc degree in Life Science or a related disciplines and at least one year of experience.
GMP background including working knowledge of GLP/GMP.
Supervisory, written and oral communications skills.
Organizational and project management skills. Analytical and balanced decision-making skills.
Familiar with QMS, LIMS, and SAP. Affinity for digital.
Ability to multi-task and adapt quickly in a fast-paced environment with evolving priorities and tight deadlines.
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 is now open for applications.
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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Pursue progress. Discover extraordinary.
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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
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