CMC Dossier Lead for Regulatory Submissions
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Johnson & Johnson is seeking a Principal Scientist, Chemistry, Manufacturing & Controls (CMC) Dossier Development. You will develop technical eCTD sections for regulatory CMC dossiers, coordinate timeline and document generation, and lead dossier authoring with managerial support.
You will interact with Regulatory, project teams and external partners to ensure compliant submissions. The role requires a PhD or equivalent with 3+ years post-doc or a Bachelor's/Master's with 6+ years in pharma,