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
Robust organizational and project management skills
Ability to work in a team-oriented team setting Drive regulatory excellence and contribute to Freyr's mission while advancing your career in compliance and submissions.
📌 Regulatory Compliance Specialist At Freyr Toronto
🏢 Freyr Solutions
📍 Toronto
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