Location: Mumbai
Experience: 7 - 15 years
Key Skills: DCP , DRA, "Regulatory Affairs"
Education: B.Pharm, M.Pharm, Phd
Category:Pharmaceutical/ Biotechnology
Role :Drug Regulatory Doctor
Industry
• Bio Technology & Life Sciences
• Pharmaceuticals
Job Description
1. Provide regulatory input during the development process intended for registration in European market. 2. Review and send the response to DCP / national / MRP queries as per the agreed timelines. 3. Planning and execution of dossiers for European Union. 4. To Head the Regulatory Affair department responsible for registration for European Union. 5. To Review and send a quality product registration document for product approval. 6. Resolve regulatory related issues experienced by various departments of the companies.
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Posted On: 9th Oct 2009
Job Ref Code: GM DRA
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