- Experience in developing and validating sensitive and rugged bioanalytical methods by using different extractions (i.e. SPE, LLE etc.) and quantitation (i.e. LCMS, HPLC) techniques for analysis of drug substances
- Experience in conducting sample analysis of Bioavailability/Bioequivalence Studies independently with required accuracy.
- Experience in operation, maintenance and calibration of laboratory instruments adhering to written instrument operation procedures.
- Ability to maintain GDP and GLP compliance in the laboratory.
- Know-how of current applicable regulatory requirements.