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About the Role
Develop globally aligned regulatory strategies throughout product development while collaborating with global regulatory and product teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
Responsibilities
- Serve as primary Canadian authority contact, leading meetings for assigned projects.
- Manage timely Health Canada clinical trial, marketing application and post-approval submissions.
- Develop high-quality, globally aligned regulatory strategies throughout relevant product development stages.
- Represent Regulatory Affairs on cross-functional teams.
- Ensure Canadian regulatory and local standards compliance; monitor Health Canada policy, regulation and guidance changes, providing comments.
- Develop local labelling and patient information; approve promotional and non-promotional materials against regulatory requirements.
- Support Health Canada Drug Establishment License activities and local/global process development.
Requirements
- Scientific bachelor’s degree; advanced degree preferred.
- 6–8 years’ regulatory experience leading submissions and obtaining clinical trial application, New Drug Submission and post-market submission approvals.
- Experience leading face-to-face Health Canada meetings and new product launches.
- Strategic thinking and clinical advice based on local requirements.
- Problem-solving, multitasking and prioritisation abilities.
- Excellent verbal, written and interpersonal communication.
- Collaboration in an innovation-focused matrix environment.
- French and English bilingualism is an asset.
Location
- Toronto
Work Type
- Hybrid
Experience Level
- Senior Manager
Education Level
- Bachelor's degree
- Advanced degree preferred
Benefits
- Annual bonuses or other incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Insurance benefits (e.g. medical, dental, vision, life and disability)
- Paid time off
- Family support benefits
About the Company
- Regeneron uses science and innovation to develop life-changing medicines for people with serious diseases.
Equal Opportunity
- Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.
- Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.