CMC Dossier Lead Scientist – Regulatory Submissions

Il y a 3 jours

Geel, Antwerpen, Belgique 7555-Janssen Pharmaceutica NV Legal Entity Temps plein 83 000 € - 165 000 € Contrat

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.