Preparation and modifications of Specifications Standard test procedures Raw data sheets analytical reports and Certificate of analysis.
Maintaining cGLP cGMPGDP and safety in quality control dept.
Involved in nonroutine activities like maintaining laboratory standards calibration of instruments.
Review of all QC related instruments calibration documents.
Responsible for Review and release of Batch Records.
Review and approval of Change controls Corrective actions and preventive actions CAPA Exceptions Investigations.
Validating new methods and scale up from pilot batches to manufacturing batches.
Developed analytical method for tablet containing different type of formulation by HPLC and UVSpectrophotometric Method.