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. #J-18808-Ljbffr

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