Cadila Pharma

•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 clear 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.

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Skills Required

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