Asst Manager- Regulatory Affairs – Baddi – India

Full Time
Job Description

Job Description
 

        Strong with Regulatory documentation
        MFR/SOP/AMV(analytical Method Varidation),ACTD/CTD, Dossier Preparation
        Having a sound knowledge of COPP preparation, application filing and grant
        Will be responsible for handling Regulatory affairs Documentary requirements.
        He should have sound knowledge and experience in ROW Markets, African Countries and South East Asia.

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
Keyskills
Regulatory Affairs
CTD MFR
D
Documentation
Pharmaceuticals
pharma
QA
Quality Assurance
Regulatory
compliance
RA

3368