Execution and compilation for process validation, validation activities and compile the report, equipment qualification and utility validation Responsible for validation and qualification activity as per cgmp. Responsible for filter validation activity, cleaning validation and hold time study and media filling…
Daily monitoring of stability chambers and handling of stability study of products. Preparaing of stability protocols and schedule. Preparation of summary reports of stability study & review of batch records Responsible for ipqa monitoring, line clearance & inprocess checks at…
Responsible for analytical development for us market. Execution and compilation validation of solid oral dosage form. Handling of uv, hplc, gc & others. M.Pharm M.Sc 3 TO 6 Years Indrad Plant