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The opportunity
Publishing Associate I, Regulatory Submissions ManagementScarborough, Ontario (Hybrid)Full-time | Permanent
Teva Canada is seeking a detail-oriented and motivated Publishing Associate I to join our Regulatory Submissions Management team. In this role, you will be responsible for the publishing and dispatch of both basic and complex lifecycle management eCTD submissions, ensuring technical validation and compliance with internal and external standards.
You will work independently on document-level publishing activities, troubleshoot formatting issues, and perform quality control checks to ensure submission readiness. This role requires a solid understanding of publishing tools, document management systems, and regulatory requirements.How you’ll spend your day
Publish and dispatch major and routine lifecycle management eCTD submissions
Perform document-level publishing, troubleshoot issues, and conduct quality control checks
Collaborate with scientific and regulatory teams to plan, prepare, and review submissions
Participate in Global Regulatory Affairs project teams
Maintain up-to-date knowledge of internal and external publishing standards
Ensure compliance with Teva’s Safety, Health, and Environmental policies
Support additional projects and tasks as assigned