Pfizer is seeking a Senior Associate for the RIO Execution Hub to manage end-to-end regulatory dossiers across multi-regional, regional, and national levels, from initial registrations to product withdrawal. Hybrid work location with emphasis on timely, compliant, and efficient submissions and lifecycle support.
Responsibilities include QA reviews, local document authoring, and collaboration with submission hubs to align with regulatory strategies and launch plans.
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📌 Regional Regulatory Submissions Senior Associate (Ciudad de México)
🏢 Pfizer
📍 Ciudad de México
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