Priya Choudhari Email & Phone Number

Mumbai, Mh, In

1. Basics of analytical method development and validation of the same for quantification of drug and its impurities in various pharma & consumer products such as solids, semisolids, & liquids for regulated markets.2. Preparation of analytical validation protocol, Creation of various technical documents, stability reports, graphs, data analysis and presentations on project work.3. Validation of analytical methods for active pharmaceutical ingredient and its quantification in formulations using ICH guideline.4. Provide support to regulatory team on various submissions with appropriate data and reports.5. Documentation practice as per ALCOA++ principle, compliance with quality requirements for raw data entry and LIMS entries.6. Stability study of drugs/formulations as per ICH guidelines.7. Calibration of various analytical instruments like HPLC, UV-Visible, FTIR, IR Moisture balance, weight balance etc.8. Calculation of analytical results and preparation of the reports.9. Follow laboratory guidelines like Good laboratory practices(GMP), regulatory guidelines, quality systems- change control, CAPA, OOS investigation, Deviation etc.10. Ensure the safe environment at work place and follow ethics and data integrity principles

Hyderabad Area, India

1 Validation of analytical methods for active pharmaceutical ingredient and its quantification in formulations using ICH guideline.2 Documentation practice as per ALCOA++ principle.3Stability study of drugs/formulations as per ICH guidelines.4Calibration of various analytical instruments like HPLC, UV-Visible, FTIR, IR Moisture balance, weight balance etc.5Calculation of analytical results and preparation of the reports. 6Preparation of protocols and writing reports on experimental work. 7Follow laboratory guidelines like Good laboratory practices and ensure the safe environment at work place

Master'S Degree, Medicinal And Pharmaceutical Chemistry

Bachelor'S Degree, Pharmacy, First Class