Quality Control
Current-Perform routine analysis of raw materials, intermediates and finished products according towritten procedures and official compendia in compliance with cGMP, environmental and safety regulations. Support Quality Control (QC) and Analytical Research and Development (ARD) work carried out at USPharma Ltd-Perform routine analysis of long term and accelerated stability studies. Perform testing of raw materials, components, in-process materials, drug substance, drug products and Stability samples using instruments such as HPLC, GC, FTIR, Dissolution apparatus-Operate, maintain, qualify and calibrate the instruments/equipments associated with testing. Order and maintain laboratory supplies and purchasing records.- Write SOPs and Standard Test Procedures- Work on Method Validations and support Cleaning Validation.- Write/ Design protocols, conduct training.