Senior CMC Dossier Lead – Regulatory Science
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Johnson & Johnson Innovative Medicine seeks a Senior Principal Scientist, CMC Dossier Development, to lead technical eCTD sections and regulatory submissions for marketing and clinical trial filings. You will coordinate document generation, oversee timelines, and ensure regulatory compliance.
The role requires strong leadership, communication, and collaboration across Regulatory, Tech, Supply Chain, and external partners to drive innovative solutions in a complex regulatory landscape.