Cadila Pharma

New Product evaluation and regulatory assessment as per WHO PQ and Russia - CIS.
 To review Registration and Requalification Dossiers before submission in WHO PQ and also its
expansion in other emerging market requirement as per collaborative procedure.
 To review Registration and Re-Registration Dossiers before submission in all CIS countries.
 To maintain Country-wise registered products status for all CIS 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 CIS
countries.
 To clear issues of Commercial Orders related to Regulatory department for CIS countries.
 To guide and give support for tenders to International SBU as per regulatory requirement (if any)
for CIS countries.
 To review and resolve queries related to Contract manufacturing product.

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