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
Solid communication and problem-solving capabilities

Utilize your regulatory expertise to enhance lifecycle management for five key products in Canada.
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📌 Lifecycle Management Consultant In Regulatory Affairs Winnipeg (Canada)
🏢 G&L Scientific
📍 Canada