- Analyzing RM/In-Process/FPs/PM
- Analysis of Stability samples, preparing data for regulatory submissions
- Maintaining Proper documentation like Instrument Logs of Analysis done in accordance with GLP, cGMP guideline, Raw Data, etc
- Well versed with the Lims Software & Empower 3.
- Exposure of Regulatory Audits like US FDA, MHRA, and WHO and many customer audits
- Updating all equipment logs and registers
Qualification: B.Pharma, M.Pharma/MS/M.Sc – Chem/BioChem
Experience: 2-7 Yrs