Shape the regulatory landscape as a Regulatory Affairs Consultant focused on the lifecycle of five products marketed in Canada. Your role emphasizes strategic submission management and Health Authority interactions.

You will provide embedded support, leveraging your Canadian regulatory experience to manage submissions and ensure compliance with Health Authorities. Your strategic thinking and project management skills will facilitate seamless coordination of activities, ensuring alignment with regulatory expectations throughout the lifecycle management of these products.

Key Responsibilities:
• Act as the primary regulatory support for five marketed products
• Manage and develop regulatory submissions and supplements
• Oversee interactions with Canadian Health Authorities




• Coordinate cross-functional inputs for aligned deliverables
• Provide ongoing regulatory support throughout lifecycle

Requirements:
• Extensive experience in Canadian Regulatory Affairs
• Expertise in managing submissions and developing strategy
• Proven liaison skills with Health Authorities
• Robust organizational and communication skills
• Ability to work collaboratively within client teams

Bring your regulatory expertise to enhance lifecycle management and compliance for five vital products.
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📌 Regulatory Affairs Expert for Product Lifecycle (Manitoba)
🏢 G&l Scientific
📍 Manitoba