Quality Assurance - Vergo Pharma Research Pvt. Ltd - Goa
(2024-02)
Working in quality assurance department
- Responsible to follow good documentation practices
- Responsible for master of documents and issuance of documents to other departments (BMR, BPR, SPECIFICATION, STP, TDS, SOP)
- Responsible for the preparation of vendor performance documents
- Responsible to operate Q-ontrack software
- Responsible for the preparation of Annual Product Quality Review
- Responsible for the preparation of SOP
- Handling trainings on SOP's
Laboratory Professional - Pfizer Limited Verna Goa - Verna, Goa
(2022-12 - 2023-12)
- Responsible for following of GLP (good laboratory practices)
- Responsible for testing of raw material in laboratory
- Responsible for testing of packaging materials
- Responsible for testing of validation samples also stability samples
- Handled instruments like balance, pH meter, UV visible spectrophotometer, Polarimeter, friabilator, Disintegration tester
- Responsible for calibration of analytical weighing balance and pH meter
- Worked on generation of master data in 3.8 E caliber lims
Trainee in Packaging Development Department - Lupin Limited Verna, Goa - Verna, Goa
(2021-07 - 2022-08)
- Responsible for preparation and review of Batch Packing Records
- Responsible for preparation of CCP proposal for BPR revision
- Responsible for checking and approval of shade cards with approved Artworks from AMS system
- Responsible for preparation of BOM screenshot (Bill of Materials). Responsible for all QA documentation
- To operate SAP system (System Application and Product in Data Processing). Responsible for follow GMP & GDP
