Responsible for to plan and perform the analysis for Finished product method validations and analytical method verifications.
Responsible for Preparation of protocols and summary reports for analytical method validations and analytical method verifications as per the regulatory requirements.
Responsible for analytical method transfer from Analytical Development to Quality Control Department in co-ordination with Quality Control.
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.
Responsible to perform the analysis for method equivalency, Pharmacopoeial updates and to address the regulatory queries.
To support Formulation Development by performing in-process, finished product analysis.
To perform the Calibrations of analytical equipments/Instruments as per the SOP.
Following all the Good laboratory practices, Good documentation practices and safety rules and regulations in the premises.