+ Responsible to work as per the organizational compliance requirement. + Responsible to develop the method for different quality attributes for complex injectable drug products like Liposomes, Ophthalmic Drug product. + Responsible to perform method validation & verification + Responsible to perform analysis of drug product by using different analytical techniques like HPLC, GC, UV, and other relevant techniques. + Responsible to perform Identification, Investigation and troubleshooting task. + Responsible to perform chemical analysis like, Extraction, Refluxing, Residue on ignition, Centrifuging & Evaporation etc. + Responsible to prepare the study template, analytical method validation & verification reports & protocols. We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.