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To perform Comparative, multimedia, discriminatory and other relevant dissolution activity for Drug Product as per regulatory requirement. |
To perform Method validation of drug product for Assay, RS, Dissolution etc. |
To perform calibration of Laboratory instruments. |
Preparation of protocol, Test Data Sheet and Report for Method Validation. |
To maintain the GLP practice in the Laboratory. |
| Wet Analysis |
1-3 Years of related experience
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