CMC Dossier Lead Scientist – Regulatory Submissions
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Johnson & Johnson in Belgium seeks a Senior Principal Scientist for CMC Dossier Development to craft technical eCTD sections and lead dossier authoring for regulatory filings. You will coordinate timelines and resources with cross-functional teams to ensure compliant submissions.
The role requires PhD with 6+ years or a Master's/Bachelor with 8+ years in chemical/biological/pharma, plus extensive experience with CMC submissions and FDA/EMA guidelines.