Naprod’s vision is to become a world class player in oncology through excellence in innovation, discovery of new manufacturing processes / drug delivery mechanisms and consistently high quality of production. We commenced operations in 1994 with the inauguration of our ultra-modern facility for the production of generics and formulations for oncology and other therapeutic applications. We are one of the pioneers in India in lyophilization.
Post: Officers - Regulatory Affairs
Job Description:
CANDIDATE'S RESPONSIBITLIES SHALL BE;
1. DOSSIER PREPARATION CTD AND ACTD FOR REGULATED MARKET.
2. PREPARATION OF DOSSIER FOR REGULATED MARKET.
Desired Profile:
SUCCESSFUL CANDIDATE IN M.PHARM WITH MINIMUM 2 YEARS EXPERIENCE IN CTD DOSSIER PREPARATION CAN APPLY.
SHOULD BE AWARE OF VARIOUS COUNTRIES REGULATORY GUIDELINES.
PHARMA FILED EXPERIENCE SHOULD BE AN ADDED ADVANTAGE.
CANDIDATE WHO CAN TRAVELL IN MIRA ROAD ONLY NEED TO APPLY.
Additional Information:
Experience: 2-4 Years
Location: Mumbai
Education: B.Pharm, M.Pharm
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: DRA
End Date: 30th sept., 2011
Forward your resume at, ranjith.kaithakkal@naprodgroup.com
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