Advance your career as a Regulatory Affairs Manager at AstraZeneca, where you’ll oversee regulatory projects on a challenging 9-month contract. Drive excellence in regulatory submissions while working collaboratively. In this role, you will need a background in science and 2-4 years of regulatory experience in the biopharmaceutical industry.

Your responsibilities include developing strategic submission plans and ensuring compliance with health authority requirements. As a project manager, you will lead cross-functional teams, analyze regulatory risks, and mentor fellow professionals. Key Responsibilities:

- Lead planning and execution of regulatory submissions
- Review and refine documents for submission accuracy




- Analyze and recommend strategies for health authority interactions
- Update and maintain project plans effectively
- Coach and support team members in regulatory processes Requirements:
- Relevant University Degree in a scientific discipline
- 2-4 years of Regulatory Affairs experience
- Robust leadership and project management skills
- Knowledge of AZ processes and drug development
- Excellent communication and analytical abilities Utilize your regulatory insights and project management acumen at AstraZeneca to foster innovation and collaboration in healthcare solutions.

📌 Regulatory Affairs Manager Contract at AstraZeneca (Mississauga)
🏢 AstraZeneca
📍 Mississauga