Dr. Reddy's Laboratories Needs Regulatory Affairs Specialist

Candidate Profile:
Work with Regulatory Agency(ies)/Consultants to derive/endorse key regulatory/clinical strategy(ies) – During R&D, pre- dossier submission, post-dossier submission
Review, compilation and submission of dossiers.
Collaborate and drive regulatory approvals with the local (India) and international regulatory body(ies).

Additional Information:
Experience: 2-6 Years
Education: B.Pharm, M.Pharm
Location: Hyderabad
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Last Date: 30^th Sept., 2011

You may share your profile at the following email address: tatipdo@drreddys.com