Responsible to perform the analysis of in-process samples such as blend assay, content uniformity, water content/LOD to support the Formulation Development.
Responsible to perform the analysis of Finished product and Stability samples such as Assay Related substances, uniformity of dosage units, Dissolution, water content/LOD etc,
To perform the dissolution profile in different medias for Finished product for regulatory submission and to support the bio study.
Responsible for conducting the experiments to develop the analytical methods, such as Assay, Dissolution, Residual solvents, Related Substances etc., for Finished dosage forms and also responsible for the Residue method and PSD method development for raw materials.
To perform the solubility studies at different PH for the drug substance as per the requirement of Formulation development.
To perform the analysis for pre-formulation samples and hold time study samples.
Responsible for the preparation of Working Standards.
To perform the Calibrations of analytical equipments/Instruments as per the SOP.
Preparation of Test methods, Development reports, Miscellaneous reports and SOP.
Following all the Good laboratory practices, Good documentation practices and safety rules and regulations in the premises.