Regulatory Affairs
Designation Level : Officer/Executive
Experience Required : 3 to 6 years
Education : B. Pharm / M. Pharm
Job Location : Padra , Dist : Vadodara,Gujarat
For CMC reviewer and compilation
-Compilation and submission of eCTD dossier for new product application (ANDA/EU-MA)/Post approval submission to the regulatory authority (specifically EU/US)
-Hand on experience in preparation of CTD section as per regulatory requirements of different region
-Having experience in preparation of query response and PAS, CBE and annual report.
-Have ability to co-ordinate with cross functional team
-Having experience for Drug listing and annual updates
-Having ability to review documents as per current regulatory guidelines.
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