High Salary Manager 1

3 weeks ago


Vadodara, Gujarat, India Sun Pharmaceutical Industries Full time

Preparation of registration strategy for various health authorities of other Latin American countries i e Peru Ecuador Colombia Panama T T DMRP Jamaica Adequate understanding on respective authority guidance and filing of new product and post approval changes Review of documents related to product registration and dossier submission leading to faster approval Prepare response to deficiency letter received from various agencies Maintain life-cycle post approval changes for drug product registration dossiers including timely circulation of approval information Provide regulatory support to cross functional department Adequate assessment of change control as per regulatory guidance Prepare and submit scientific advice to various health authorities Job Location Baroda



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