Join Cerapie Pharma as a Regulatory Affairs/Product Registrations Manager in Mississauga, ON, focusing on product registration and compliance with pharmaceutical regulations. Your expertise will drive submissions and maintain regulatory standards.

In this full time, on-site role, you will be pivotal in preparing and coordinating regulatory applications for both Canadian and international markets. You will collaborate with internal departments to ensure that documentation reflects rigorous regulatory requirements while staying ahead of any changes. Your input will be vital in supporting audits and inspections for product integrity.

Key Responsibilities:
• Plan and submit regulatory documentation for product registrations
• Track and manage regulatory submission timelines efficiently




• Maintain and update regulatory documentation and dossiers
• Respond to health authority queries as needed
• Collaborate with multiple teams to uphold compliance

Requirements:
• In-depth knowledge of Canadian and international regulations
• Proven experience in regulatory submissions and document management
• Bachelor's degree in Pharmacy, Life Sciences, or related fields
• Strong analytical skills and attention to detail
• Previous pharmaceutical experience in regulatory affairs

Advance Cerapie Pharma’s commitment to quality through expert regulatory management.
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📌 Regulatory Affairs/Product Registrations Manager (Ontario)
🏢 Bilinguallink
📍 Ontario