Take a pivotal role as a Regulatory Affairs Coordinator at UBC's Advanced Therapeutics Manufacturing Facility, where your expertise in regulatory submissions will drive innovation. This position requires a meticulous approach in a GMP-focused setting.
The successful candidate will manage the regulatory process for advanced therapeutic products, aligning with Health Canada, FDA, and EMA guidelines. Collaborating with multidisciplinary teams, this hands-on role involves preparing extensive documentation and ensuring compliance with regulatory standards essential for clinical trials. Your work will support key advancements in health therapies across Canada.
Key Responsibilities:
• Oversee regulatory submissions and manage documentation
• Evaluate compliance with health regulatory standards




• Collaborate with cross-functional teams for submission readiness
• Address inquiries from health authorities efficiently
• Monitor evolving regulations and adapt processes accordingly
Requirements:
• Undergraduate degree in a relevant discipline
• Minimum of three years relevant experience
• Knowledge of GMP and submission processes
• Experience with regulatory interactions in biotech
• Effective communication and project management skills
Leverage your regulatory expertise to impact health innovation at UBC and drive the future of advanced therapeutics.
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📌 UBC Regulatory Affairs Coordinator Role (Vancouver)
🏢 University of British Columbia
📍 Vancouver