Ensuring all products coming under Pharma Division are duly licensed/registered and abide to the local acts and other relevant regulations up to the point of releasing the products to the market and monitoring the same afterwards related to quality and Adverse Events (AE). Selected candidate will be responsible for procuring documents from principals, evaluating the same, preparing dossiers, working on additional, notifying and submission to NMRA and following up the same when necessary.

Note: Your CV should be in .doc, .docx or PDF format and less than 3MB