Join AstraZeneca as a Regulatory Affairs Manager, specializing in project management within regulatory affairs on a 9-month contract. Contribute to impactful regulatory submissions in a collaborative setting. This position requires a relevant science degree and 2-4 years of regulatory experience, offering a chance to guide submission strategies and improve processes.

You will work closely with cross-functional teams and engage with health authorities while managing procedures for various applications. Your analytical skills will be essential in identifying risks and enhancing documentation practices. Key Responsibilities:

- Manage regulatory submission processes from strategy to delivery
- Liaise with health authorities and document key requirements




- Prepare and review documents for regulatory compliance
- Develop and maintain submission delivery plans
- Provide mentoring and support within team initiatives Requirements:
- Relevant University Degree in Science
- 2-4 years of industry regulatory experience
- Sound knowledge of drug development
- Proven project management capabilities
- Robust influencing and analytical skills Leverage your regulatory expertise to enhance AstraZeneca's high-quality deliverables and make a lasting impact.

📌 AstraZeneca Regulatory Affairs Manager Role (Mississauga)
🏢 AstraZeneca
📍 Mississauga