To perform sample processing, quantification for Method development and Method validation for various molecules for which In-vitro studies needs to be conducted following the SOPs, protocol and regulatory guidelines.
To conduct study sample analysis and quantification of the In-vitro study samples following the validated analytical procedure, protocol and applicable regulatory guidelines.
To conduct the calibration of equipment’s used in Bioanalytical department as per the respective instrument SOPs.
To document the method development activities in Lab note Book, sample preparation details in the raw data forms generated during course of Method validation and In-vitro study sample analysis.
Implementation of Quality systems and SOP's .
Any other responsibilities assigned by Head-Bioanalytical.
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