Global Regulatory Affairs Vaccines Strategist - VIE Contract

Sanofi; Toronto; On-site; CAD 50,000 - 90,000; Full time

Job summary

Join an innovative global healthcare company as a Global Regulatory Affairs Vaccines Strategist. This role offers a unique opportunity to shape the future of medicine by supporting regulatory activities for vaccines. You will coordinate efforts across teams, ensuring compliance and facilitating product licensing in Canada and beyond. With a commitment to investing in young talent, this position provides real responsibilities and growth potential in a collaborative environment. If you are passionate about making a difference in public health, this is the perfect opportunity for you.

Qualifications

• Experience in Regulatory Affairs is a strong asset.
• Experience in the pharmaceutical industry is highly preferred.

Responsibilities

• Coordinate regulatory activities supporting CTD and Global Submission Plan.
• Assist in the preparation of consultations with authorities.

Skills

MS Office (Excel)

Communication Skills

Coordination Skills

Organizational Skills

Multitasking Abilities

Team Orientation

Education

Master’s degree in Biology

Master’s degree in Life Sciences

Master’s degree in Regulatory Affairs

Tools

Think Cell

Job description

Global Regulatory Affairs Vaccines Strategist - VIE Contract

Location: Canada, Toronto

Target start date: 01/09/2025

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein, and Iceland) aged between 18 and 28.

Note: Since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

Note: Applications submitted only in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Only applications in English will be considered. Please ensure you apply with your personal email address.

About the job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our Regulatory Affairs team as Global Regulatory Affairs Vaccines Strategist VIE and participate in the missions of the Global Regulatory Affairs Franchise Vaccines Traveler Endemic.

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. Our talented teams explore new technologies to protect people and promote healthy communities, making a real impact on millions of patients worldwide.

Main responsibilities:

Global Tasks:

• Coordinate regulatory activities supporting the Common Technical Documents (CTD) task force, including pre-submission activities.
• Coordinate regulatory activities supporting the Global Submission Plan with the global product regulatory team (GRT), track and update the Global Simultaneous Submission plan (GSS).
• Participate in the preparation of consultations with authorities.
• Support the Global Regulatory Lead (GRL) for meetings of the global regulatory team (GRT), including preparation, meeting minutes, and follow-up actions.
• Assist the update of the Global Regulatory Product Strategy (GRPS) document.

Specific Country Tasks:

• Coordinate and contribute to regulatory activities for dedicated products.
• Collaborate with Canadian GRL and RS to support product licensing in Canada, the US, and worldwide, including new market authorizations, line extensions, and labeling variations.

About you

Experience:

• Previous experience in Regulatory Affairs is a strong asset.
• Experience in the pharmaceutical industry is highly preferred.

Skills:

• Advanced MS Office skills, especially Excel; Think Cell is a plus.
• Good communication, coordination, and facilitation skills.
• Excellent organizational and multitasking abilities.
• Strong team orientation.

Education

• Master’s degree in Biology, Life Sciences, Regulatory Affairs, or related fields.

Languages

• Proficiency in English.

Why choose us?

iMove is a unique program tailored for European youth interested in challenging themselves with meaningful international assignments. Sanofi is committed to investing in young talents who will drive our future success.

Sanofi’s Work Abroad Program, iMove, offers roles with real responsibilities and growth potential across various functions such as marketing, finance, regulatory affairs, supply chain, clinical trials, and production in over 40 countries. Join us to make a difference through your work.