To work in API check daily all documents like BMR, BPR, ECR, weighing calibration records.
Work with proper WHO GMP Guidelines.
To make COAs (Certificate of Analysis) for batch release
Implement documentation system to develop, maintain, distribute and control all Quality Control, Quality Assurance, Production, Maintenance and Warehouse records
IPQA (In process Quality Assurance)
BPR Checking, BMR Checking, MFR Preparation
Handling of Change, Control & Deviation
Document Issuance to other departments
Filled Vendor Questionnaire
Work with proper GDP
Excellent communication skills.
B,Pharma, QA, Quality analyst, pharmaceutical, science graduate, M.Pharma
Posted on: 2nd Jun, 2020