job title: team member - regulatory affairs(cipla)

Job Purpose

1. Coordination for dossier checklist, preparation and submission, follow-up for timely regulatory approval and response submission.

2. Participate in discussions and coordinate with RA/IPD/Portfolio/Medical Affairs/Marketing team to obtain all the necessary documentation specific to products in compliance to regulatory requirement. 

   Education Qualification

   B. Pharm/M.Pharm/ other regulatory certified courses will be preferred.

   Relevant Work Experience 

   Threshold skills and capabilities required to execute the role: Technical knowledge of India Regulatory landscape, inter-personal skills

   Relevant experience: Minimum 5-10 years of experience in Regulatory Affairs