Regulatory Affair Associate - (Quality/Regulatory)
20 days ago
Totowa
Assist the Manager of Regulatory Affairs during cGMP, Environmental, and Regulatory audits.With the assistance of Head of R&D (or designee), create and collate product master files (dossiers), drug master files (DMF).Generate and Review of Product CoCs, CoAs, CoMs, BSE documents, CMR documents, ....