Executive - Regulatory Affairs (Sun pharma)

Roles and Responsibilities

Key Responsibilities:

• Compilation , review of dossier for US , EU , AU, Canada & IL market for both solid oral and non-oral dosage form

• Review of query response prepared and compiled by regulatory associates

• Manage all the activities pertaining to dossier submission for aforesaid markets .

• Meet the dossier submission and query response timeline as per given target

• Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management

• Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities

• Lifecycle management for US , EU, Canada & IL market

• Single point contacts for all the regulatory submission activities for IL and Palestine markets

Travel Estimate

NA

Job Requirements

Educational Qualification

M.Pharm

Experience

Tenure: 2 – 4 yrs.