Join as a Regulatory Affairs Consultant focusing on lifecycle management for five marketed products in Canada. Your expertise will drive effective regulatory submissions and Health Authority interactions.
As an experienced consultant, you will provide embedded Canadian Regulatory Affairs support across various products. This role emphasizes developing regulatory strategies, managing submissions, and liaising with Health Authorities for effective interactions. Your experience with project management and regulatory submissions will be crucial in ensuring timelines and compliance.
Key Responsibilities:
• Provide Canadian Regulatory Affairs support for five products
• Lead development and management of regulatory submissions
• Develop strategies for complex regulatory submissions
• Act as liaison with Canadian Health Authorities
• Manage submission activities throughout the lifecycle
Requirements:
• Robust experience in Canadian Regulatory Affairs
• Familiarity with marketed pharmaceutical products
• Proven ability in submission development and management
• Excellent project management and coordination skills
• Strong communication and problem-solving capabilities
Utilize your regulatory expertise to enhance lifecycle management for five key products in Canada.
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