Executive Regulatory Affairs, Pharmaceuticals

3 - 6 Years

Job Description

- Review of documents received from CG - Facilitating preparation of BMR, BPR, PVP, specs, protocols, artworks, mock-ups - Coordinating with CG for review and approval of documents, change controls, qualification - Submission of variation in dossiers

Salary: Not Disclosed by Recruiter

Industry:Pharma / Biotech / Clinical Research

Functional Area:Legal, Regulatory, Intellectual Property

Role Category:Drug Regulatory Affairs/Documentation

Role:Regulatory Affairs Manager

Employment Type:Permanent Job, Full Time

Key Skills

Desired Candidate Profile

Please refer to the Job description above

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