Cadila Pharma

To ensure Registration dossier submission of products in different SEA countries (Region II), Africa countries (Region I) as per agreed timeline.

To ensure Renewal of registered product prior to validity expiration of SEA countries (Region II),Africa countries (Region I).

To Review Registration and Re-registration dossiers before submission in all SEA countries (Region II),Africa countries (Region I)

To maintain country-wise registered product status for all SEA countries (Region II),Africa countries (Region I)

To co-ordinate with other departments R&D, QA and QC for ensuring the filings & query responses.

To provide technical support to team for preparation of Registration/Re-registration dossiers and query responses.

To prepare documents for variation filings as and when required for all SEA countries (Region II),Africa countries (Region I)

To update registration information in SAP & Cadinet for SEA countries (Region II),Africa countries (Region I)

To clear issues of commercial Order related to regulatory department for SEA countries (Region II),Africa countries (Region I)

To review the tender requirements and extend necessary support by providing the required documents and samples.

To co-ordinate with International country managers for smooth scheduling the registration activity.

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Skills Required

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