Freyr seeks a skilled Regulatory Affairs Specialist in Toronto, ON to support Canada's pharmaceutical regulatory compliance remotely. Become a key player in ensuring timely submissions to Health Canada.
Join Freyr, a global leader in regulatory solutions, as a Regulatory Affairs Specialist focused on supporting pharmaceutical operations in Canada. Your role involves preparing and coordinating regulatory submissions, addressing inquiries, and maintaining compliance with Health Canada’s regulations. Collaborating with diverse teams will be vital for achieving successful outcomes while enhancing your expertise in regulatory processes.
Key Responsibilities:
• Compile and review regulatory dossiers for Health Canada
• Manage various submission types, including SNDS and CTA
• Co-manage responses to regulatory information requests
• Monitor compliance and regulatory policy updates
• Ensure quality standards for regulatory documentation
Requirements:
• Bachelor's degree in a relevant field
• Minimum of 5 years’ experience in Regulatory Affairs
• Hands-on experience with Health Canada submissions
• Solid understanding of lifecycle management
• Excellent attention to detail and communication
Support vital submissions and thrive in your regulatory career with Freyr, making a real-world impact in the life sciences.
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