Regulatory Affairs Project Leader

(0609) sanofi-aventis Canada Inc.; Toronto; On-site; CAD 181,000 - 252,000; Full time

Job summary

Sanofi Group in Toronto, ON is actively seeking a Regulatory Affairs Project Leader to drive regulatory strategy and filings for our Health Canada portfolio. You will coordinate with Health Canada and internal teams to develop filing strategies and ensure compliant submissions across product lifecycles.

The role requires a BSc and 2–3 years of Regulatory Affairs experience, with strong knowledge of Health Canada regulations and PAAB guidelines.

Qualifications

• Education: BSc (required) or degree in a health-related field.
• 2–3 years of Regulatory Affairs experience.
• Strong knowledge of Health Canada regulations and PAAB guidelines.
• Ability to lead major submissions and work with cross-functional teams.

Responsibilities

• Provide regulatory strategy and operational input to local and global teams for development and marketed products throughout their lifecycle.
• Develop and execute filing strategies, including summarizing scientific/clinical information where applicable.
• Organize and coordinate meetings with Health Canada.
• Ensure high-quality regulatory submissions meet timelines and regulations.
• Coordinate cross-functional meetings, providing SME input on product strategies.
• Maintain compliance for marketed products including label updates.
• Review and approve promotional and non-promotional material per regulatory requirements.

Skills

Regulatory strategy

Regulatory submissions

Health Canada regs

PAAB guidelines

Stakeholder mgmt

Change leadership

Strategic thinking

Independent work

Education

BSc

Tools

MS Outlook

PowerPoint

Word

Excel

Adobe Acrobat

Veeva Vault

Job description

Reference no. R2876875 Position title: Regulatory Affairs Project Leader Department: Regulatory Affairs Location: Toronto, ON

About the job

Join the engine of Sanofi's mission - where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions. The Canada Regulatory Affairs team is responsible for preparing and submitting regulatory dossiers to Health Canada to ensure regulatory compliance and obtain marketing authorizations for Sanofi's General Medicine, Specialty Care, and Vaccine portfolio products. The team serves as the direct point of contact with Health Canada, coordinating regulatory submissions, responding to authority questions, and maintaining commitments to support timely product approvals.

Position Summary:

Responsible for the Regulatory Affairs (RA) project management of development and marketed products.

About Sanofi

We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system - and innovative pipeline - enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

Main responsibilities

• Provide regulatory strategic and operational input to local and global teams for development and marketed products throughout their lifecycle
• Develop and execute filing strategies, including assessing and summarizing scientific and clinical information, where applicable
• Organize and coordinate meetings with Health Canada
• Ensure the preparation of high-quality regulatory submissions in alignment with internally defined strategies to meet agreed upon timelines and in compliance with Health Canada Regulations
• Participate in cross-functional meetings with internal stakeholders (locally and globally), providing subject matter expert input on product strategies
• Ensure the ongoing compliance for marketed products, specifically through product monograph and label updates/revisions
• Review and approve promotional and non-promotional material in accordance with regulatory requirements
• Maintenance of internal databases in timely manner as required for portfolio of products

About you

Education: BSc. (required), or a degree in a health-related field

Experience: Minimum of 2-3 years of experience in Regulatory Affairs

Specific Skills / Competencies

• Demonstrated success in a regulatory environment (e.g., leading a major submission)
• Good knowledge of the current Health Canada regulations and PAAB guidelines
• Developed change leadership skills (i.e., ability to cope with and adapt to change, effectively prioritize, and deal with ambiguity)
• Strong strategic and operational thinking (i.e., able to think big picture balanced with strong analytical skills)
• Able to manage and influence key stakeholders
• Fosters innovation (i.e., embraces new insights, concepts, trends & processes)
• Works well independently as well as in a group environment

Languages

• English (written and spoken)
• French is an asset

Computer knowledge

• MS Outlook, PowerPoint, Word, Excel, Adobe Acrobat Veeva Vault database familiarity is an asset

Travel: Occasional

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 an existing vacant role that is now open for applications.

AI Usage

"Artificial Intelligence" refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. These systems may process personal information to identify patterns, improve services, or support decision-making. These systems may process personal information monitoring.

You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada's Privacy Officer via Sanofi's data subject request portal, Data Subject Rights Webform. The Data Subject Rights Webform can also be used to request access or correction of your personal information and file a complaint.

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.

#GD-SA #LI-SA #LI-Onsite Pursue progress, discover extraordinary 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 ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

North America Applicants Only

The salary range for this position is: 127,000.00 - 177,000.00 (Includes target bonus) Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefits programs, and additional benefits information can be found through the (CA)LINKOR (US) LINK. La fourchette salariale pour ce poste est la suivante: 127,000.00 - 177,000.00 (Comprend le bonus cible) La rémunération finale sera déterminée en fonction de l'expérience démontrée, des compétences, du lieu de travail et d'autres facteurs pertinents. Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise, et des informations supplémentaires sur les avantages sociaux peuvent être trouvées via le lien We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.

Discover more about us visiting www.sanofi.com or via our movie We are Sanofi Start a career that makes a difference. Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.