Apply on Kit Job: kitjob.ca/job/2g8vn1

Join a energetic Regulatory Affairs team as an Associate, focusing on established products. Oversee high-quality regulatory submissions to Health Canada, ensuring compliance while leveraging your regulatory expertise.
This role coordinates and manages regulatory filing processes for established products. With 2-5 years of experience in drug regulatory affairs, you’ll liaise with stakeholders and maintain adherence to Health Canada regulations. Your responsibilities will include managing submission publishing standards, supporting document workflows, and implementing process improvements to enhance operational efficiency.
Key Responsibilities:
• Maintain submission publishing process standards
• Review compilation and publishing plans for compliance




• Provide business support for regulatory document workflows
• Develop project plans for registration of submissions
• Foster awareness of Health Canada eCTD updates
Requirements:
• Bachelor’s degree in life science or equivalent
• 2-5 years in drug regulatory affairs experience
• Knowledge of Canadian Food and Drug Act
• Familiarity with eCTD and publishing tools
• Strong communication and project management skills
Utilize your regulatory knowledge and expertise to enhance the submission process effectively.
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Apply on Kit Job: kitjob.ca/job/2g8vn1

📌 Regulatory Affairs Associate - Established Products (Burlington)
🏢 Boehringer Ingelheim
📍 Burlington