Drug Regulatory Affairs -Executive

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

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