Elevate your career as a Regulatory Affairs Consultant, offering lifecycle management expertise for five key products marketed in Canada. Engage deeply with regulatory submissions and Health Authority processes.

In this embedded consultancy role, you will leverage your strong background in Canadian regulatory affairs to guide regulatory submissions and ensure successful Health Authority interactions. Your strategic approach and ability to coordinate complex activities will be pivotal in managing the regulatory lifecycle of marketed products.

Key Responsibilities:
• Provide embedded support in Regulatory Affairs for five products
• Develop and manage submissions tailored to regulatory needs
• Coordinate interactions with the Canadian Health Authority




• Manage timelines and cross-functional regulatory deliverables
• Offer continuous regulatory advice for lifecycle management

Requirements:
• Deep experience in Canadian Regulatory Affairs
• Experience in pharmaceutical lifecycle management
• Proven submission management skills
• Excellent project and stakeholder coordination capabilities
• Strong communication and problem-solving skills

Join our endeavor to enhance compliance and regulatory strategies for significant pharmaceutical products.
#J-18808-Ljbffr

📌 Consultant in Canadian Regulatory Affairs (Manitoba)
🏢 G&l Scientific
📍 Manitoba