Senior CMC Dossier Scientist
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Johnson & Johnson is seeking a Principal Scientist in CMC Dossier Development to lead regulatory dossier sections for marketing and clinical trial submissions. You will coordinate timelines, manage Quality modules, and ensure regulatory compliance across FDA/EMA guidelines while mentoring junior staff.
The role requires substantial experience in regulatory CMC submissions, strong communication, and the ability to work independently on complex projects within a global team.
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Senior Principal Scientist, CMC Dossier Development
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