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 team-oriented 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 versatile 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
Robust 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.

📌 Regulatory Affairs Director At Astrazeneca Mississauga
🏢 AstraZeneca
📍 Mississauga