- Responsible for validating the manufacturing process of generic drug products by coordinating with various departments, such as Production, Quality Control and Engineering.- Assurance of product quality by following standard operating procedures based on GMP guidelines within a manufacturing environment.- Preparation of various technical reports, such as process and cleaning validation protocols, change control qualifications and retrospective validation reports, by data collection and information acquisition through cooperation with colleagues from other departments.- Research on new guidelines and procedures in accordance to the constant progression of the industry.