2 - 7 years
2 - 6 Lacs
Posted:-1 days ago|
Platform:
Work from Office
Full Time
1. Sound Knowledge of HPLC method development, method validation for Assay and Related substance.
2. Routine Analysis of raw materials, intermediates and finished products.
3. Sound knowledge of analytical instruments like HPLC, Gas Chromatography, Infrared spectrophotometer, UV spectrophotometer, Auto titrator, Karl Fisher, Particle Size Analyzer etc. with analytical data interpretation.
4. Good hands on experience of Drug excipient compatibility study and evaluation of analytical data.
5. Sound practical knowledge of dissolution method development and method validation for different formulations and evaluation of the data.
6. Chemical / WET analysis like Titration, LOD, Solubility, Heavy Metals, ROI, Moisture content, IR analysis, UV Analysis, SOR, Melting Point, Tap Density, Potentiometer, pH Testing, Description etc.
7. Knowledge of different tests like Assay and Related Substances by HPLC, Dissolution by HPLC, Blend Uniformity, Content Uniformity, Measurement of Osmolality, Measurement of Viscosity, Particle Size Distribution etc.
8. Knowledge of UPLC method development and conversion of analytical method from HPLC to UPLC.
9. Ensure work environment clean and safe complying with safety guidelines.
Interested candidates can share resume copy of related references on nehasharma@troikaapharma.com
Regards,
Neha Sharma
Troikaa Pharmaceuticals
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