Pharmaceutical Company is seeking a Content Strategist to lead regulatory submissions, coordinate cross-functional document development, and ensure high-quality regulatory documentation for global authorities.
The role focuses on strategic content planning, timelines, and ensuring compliance with GxP, GCP, ICH, GVP, ISO, MDR/IVDR across global programs. Hybrid 3 days onsite in Mississauga, Ontario, with extensive collaboration across functions.
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