- To review Registration and Re-Registration Dossiers before submission in all Aus / NZ countries. -To maintain Country-wise registered products status for all AUS/ NZ countries. -To co-ordinate with other departments R&D;, QA and QC for ensuring the filling and Query responses. -To provide technical support to team for preparation of Registration/Re
- registration dossiers and Query responses. -To prepare and review documents for Variation filling as and when required for all AUS / NZ countries. -To transparent issues of Commercial Orders related to Regulatory department for Aus / NZ countries. -To guide and give support for tenders to International SBU as per regulatory requirement (if any) for Aus / NZ countries. -To review and resolve queries related to Contract manufacturing and due diligence, perform SAP related activity for this product.
📌 Assistant General Manager (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka
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