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Zuellig Pharma

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Associate, Regulatory Affairs

Posted Updated
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1. Review the IMS/IQVIA tagging of the materials maintained in the system.
2. Review and align the material description as per standard format .
3. Updates and encodes the Material Maintenance Clean-up monitoring file.
4. Provides assistance on report consolidation on the activities related to Material Maintenance Clean-up.
5. Performs validation of the Material maintained in the system.
6. Performs validation of the Material maintained in the system.
7. Provide updates and reports to the Regulatory Team.
8. Performs other tasks assigned by the Regulatory Team.

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