Join AstraZeneca as an Associate Regulatory Affairs Director, leading the regulatory submissions process and ensuring compliance while working flexibly in downtown Toronto. Leverage your project management skills and regulatory expertise to drive successful drug development outcomes.

As a key role at AstraZeneca, you will work within a cooperative team to manage complex regulatory applications. Your extensive regulatory experience will guide cross-functional teams through submission strategies while identifying and mitigating risks. This role promotes innovation in a flexible environment, enhancing your ability to impact global health solutions.

Key Responsibilities:
• Lead regulatory submission strategies and complex applications
• Review and provide input on essential documents




• Develop and maintain submission content and delivery plans
• Identify regulatory risks and propose mitigations
• Coach and mentor Regulatory Affairs team members

Requirements:
• Relevant University Degree in Science or related discipline
• Over 5 years of regulatory experience in biopharmaceuticals
• Strong project management and leadership skills
• Knowledge of drug development processes
• Familiarity with AI digital tools and Veeva Vault

Bring your expertise in regulatory affairs and project management to AstraZeneca, driving impactful drug development initiatives.
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📌 Regulatory Affairs Director at AstraZeneca (Ontario)
🏢 AstraZeneca
📍 Ontario