Drug Regulatory Affairs -Executive
Job Description
1. To maintain all Drug Regulatory Affairs database like Raw material specification, COA and STP, Finished Product specification,COA and STP, Packing Material specification, COA and STP, Process validation, Stability study, Analytical Method validation and Complete Dossier.
2. Preparing Dossiers, Handling Queries and answering the query in the given time line.
3. Collecting and Review of Technical documents from QC/QA/Production.
Experience – 0 -5 years
Location - Amritsar
Education-
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy
Doctorate:Doctorate Not Required
Company Profile:
Kwality Pharmaceuticals Ltd.
KWALITY PHARMACEUTICALS LTD.
6TH, MILE STONE, VILL. NAG KALAN, MAJITHA ROAD,
AMRITSAR- 143601.(INDIA)
Contact Company:Kwality Pharmaceuticals Ltd
Email Address: hrd@kwalitypharma.com
Hello Visitors. Welcome to this blog .For any queries related to pharma please feel free to contact us at on our mail pharmastuff.blogspot.com@gmail.com
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