Essential Duties and Responsibilities: |
• Experience in method validation and method transfers activity of injectable, ophthalmic drug products, drug substances, raw materials, etc. |
• Perform the method validation and method transfer activity per ICH/USP requirements. |
• Responsible for writing method validation, verification protocol, and reports. |
• Responsible for writing test method, specifications, etc. |
• Experience in the operation of handling QC major instruments like HPLC, GC, UV, IR, Auto titrator etc. |
• Perform Finished product/in-process/cleaning validation and raw material analysis independently. Complete testing within specified timeframes and document results accurately |
• Experience in integration of chromatograms through chromeleon chromatographic software. |
• Review of analytical method/ specification and prepare GAP analysis. |
• Coordinate with R&D lab for method validation/ method transfer related query/questions. |
• Responsible for writing an investigation report for OOS/OOT if any. |
• Preparation of stability schedule, Protocol and report per requirements. |
• Adhere to regulatory guidelines (e.g., FDA, ICH, GMP) and company quality standards during testing and documentation. |
• Ensure adherence to Good Laboratory Practices (GLP), Good documentation practices (GDP) and Good Manufacturing Practices (GMP) during testing procedure. |