Karnataka

Pharmacopoeial standards for Biosimilars. Development and Characterization of Biosimilars. Biotherapeutics: Regulatory landscape

SSLC & Diploma in Pharmacy from KPB

M.Pharm in the relevant specialization Ph.D. in Pharmaceutical Sciences. Applications are invited for faculty roles in the following departments- Pharmaceutics, Pharmaceutical Chemistry, Pharmacology, Pharmacy Practice, Pharmacognosy, Regulatory Affairs

Compilation of high quality Annual Product Reviews / Product Quality Reviews for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system

Comply with internal and external timelines for managing adverse events and product complaint case processing, and case submission processes as appropriate. 

In this role you are required to do analysis and solving of moderately complex problems

This role focuses on managing post-approval regulatory activities, including variations, renewals, and compliance with country-specific requirements. You will partner with cross-functional teams to ensure timely submissions and maintain regulatory dossiers.

Support system implementation, upgrades, and change management. Work with clients and crosse Functional teams to ensure regulatory compliance 

M.Sc, M.Pharm, M.Tech candidates who have qualified for the Category I or Category II merit list of DBT-BET exam or NET/GATE qualified candidates.