To support and provide assistance to Departmental Manager, in attending product registration matter, any task related to Regulatory Affairs (RA), Contract Manufacturing Organization (CMO), and Pharmaniaga Research Centre (PRC).
To assist in dossier compilation and technical documents regarding technology transfer from CMO, CRO and PRC.
To ensure dossier compilation meet Health Authority regulations and queries are attended accurately. All submissions shall adhere to project timeline.
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