Global Regulatory Affairs Vaccines Strategist - VIE Contract

Sanofi; Toronto; On-site; CAD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking global healthcare company as a Global Regulatory Affairs Vaccines Strategist. This role is pivotal in expediting drug discovery and development, impacting millions of lives through innovative vaccine solutions. The ideal candidate will have a Master's degree in a relevant field and prior experience in regulatory affairs. You will coordinate regulatory activities across various markets, ensuring compliance and supporting licensing submissions. This is an exceptional opportunity to grow professionally while contributing to global health initiatives within a diverse and inclusive environment.

Qualifications

• Prior regulatory affairs or pharmaceutical industry experience is preferred.
• Fluent in English is a must for this role.

Responsibilities

• Coordinate regulatory activities for Common Technical Documents and Global Submission Plan.
• Assist in updating the Global Regulatory Product Strategy.

Skills

MS Office

Communication Skills

Organizational Skills

Team Skills

Education

Master’s degree in Biology

Master’s degree in Life Sciences

Master’s degree in Regulatory Affairs

Job description

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Global Regulatory Affairs Vaccines Strategist - VIE Contract

Location: Toronto, ON, Canada

Target start date: 01/09/2025

Application deadline: August 29, 2025

Program eligibility: The iMove, Sanofi's VIE Program, is open to citizens of the European Economic Area (EU + Norway, Liechtenstein, Iceland) aged 18-28. Candidates cannot apply in their own country of citizenship. Applications must be submitted in English.

About the role

Join Sanofi’s innovative global healthcare team as a Global Regulatory Affairs Vaccines Strategist VIE. Contribute to speeding up drug discovery and development, impacting millions of patients worldwide. Sanofi helps prevent infectious diseases with over 500 million vaccine doses annually and explores new technologies to promote healthy communities.

Main responsibilities

• Global Tasks:
• Coordinate regulatory activities supporting the Common Technical Documents (CTD) and the Global Submission Plan.
• Participate in consultations with authorities and support meetings of the global regulatory team.
• Assist in updating the Global Regulatory Product Strategy (GRPS).

• Country-specific Tasks:
• Coordinate regulatory activities for specific products, supporting licensing and variation submissions in Canada, US, and EU markets.

Candidate profile

Experience: Prior regulatory affairs or pharmaceutical industry experience is preferred.

Skills: Proficiency in MS Office, excellent communication, organization, and team skills.

Education: Master’s degree in Biology, Life Sciences, Regulatory Affairs, or a related field.

Languages: Fluent in English.

Why join us?

Sanofi’s iMove program offers meaningful international assignments across various functions and countries. It’s an opportunity to grow professionally while making a difference in global health. We value diversity and are committed to equal opportunities.

About Sanofi

Sanofi is a global biopharmaceutical company dedicated to human health, specializing in vaccines, treatments, and addressing rare and chronic diseases. With over 100,000 employees worldwide, we’re committed to scientific innovation and healthcare solutions.