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 processesRequirements:- 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 abilitiesUtilize your regulatory insights and project management acumen at AstraZeneca to foster innovation and collaboration in healthcare solutions.#J-18808-Ljbffr

📌 Analyst, Regulatory Reporting (18 Months Contract) - $115,000 - $160,000 A Year (Winnipeg)
🏢 AbCellera
📍 Winnipeg