Lead and support groundbreaking projects in Regulatory Affairs. Develop technical knowledge while managing regulatory submissions and compliance for market products in a vibrant R&D; workplace.
This Project Leader role emphasizes experience in regulatory affairs and project management. You will provide strategic regulatory insights, coordinate meetings, and ensure timely submissions to Health Canada. Your responsibilities will contribute to the successful registration and lifecycle management of drugs and vaccines.
Key Responsibilities:
• Provide regulatory input for product lifecycle management
• Develop filing and approval strategies for regulations
• Organize meetings with Health Canada officials
• Ensure compliance with drug labels and monographs
• Review promotional materials for regulatory consistency
Requirements:
• 1-2 years experience in regulatory affairs preferred
• Master’s degree in pharmacy or life sciences required
• Strong project management and organizational skills
• Proficiency in Microsoft Office and databases
• Fluent English in written and verbal forms
Harness your regulatory expertise to drive successful drug and vaccine registrations, ensuring compliant submissions and impactful projects.
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Apply on Kit Job: kitjob.ca/job/2fs7hk
📌 Regulatory Affairs Project Leader Role (Toronto)
🏢 Sanofi
📍 Toronto
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