Join Freyr as a Regulatory Affairs Specialist in Toronto, ON and take on the challenge of managing government relations for pharmaceutical products remotely. Help streamline regulatory submissions to Health Canada.

Freyr, a reputable global provider of regulatory solutions, is looking for a Regulatory Affairs Specialist to focus on the management of regulatory submissions in Canada. You will coordinate and prepare all relevant documentation to ensure compliance with Health Canada. This position offers the chance to collaborate with multidisciplinary teams to deliver regulatory submissions effectively, helping to drive product approvals and market readiness.

Key Responsibilities:
• Prepare and submit documents to Health Canada
• Oversee administrative documentation for submissions




• Support global updates to product labeling
• Manage regulatory databases and submission trackers
• Address regulatory compliance queries or challenges

Requirements:
• Bachelor’s degree in Pharmacy, Life Sciences, or related science
• 5+ years of experience in Regulatory Affairs
• Familiarity with Canadian submission processes
• Solid organizational and project management skills
• Ability to work in a collaborative team environment

Drive regulatory excellence and contribute to Freyr's mission while advancing your career in compliance and submissions.
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📌 Regulatory Compliance Specialist at Freyr (Ontario)
🏢 Freyr Solutions
📍 Ontario