Sr.executive/assistant Manager-regulatory Affairs

4 - 6 Years

Job Description

Review of documents /data received from contract manufacturing and provide inputs to team for implementation. Preparation/review of documents including BMR, BPR, PVP, Specifications, protocols, artworks, mock-ups etc. Site Transfer, variations.

Salary: INR 3,00,000 - 5,00,000 P.A.

Industry:Pharma / Biotech / Clinical Research

Employment Type:Permanent Job, Full Time

Key Skills

Desired Candidate Profile

Candidate with B.Pharm / M.Pharm, experience of 4 to 6 years in site-transfer/regulatory/QA for EU Markets. Good communication skills and team person. Knowledge of ICH, GMP CTD and variation guidelines.


UG:B.Pharma - Pharmacy

PG:M.Pharma - Pharmacy

Company Profile

Kopran Ltd
An Indian Multinational Pharmaceutical Company with state of the art Plants for the manufacture of Active Pharmaceutical Ingredients and Finished Dosage Forms, having exports to over 50 countries.
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Contact Company:Kopran Ltd