• Assisted the development of new products and wrote patents for the company• Developed the overseas business by translating email, websites, national standards and some contracts related to the overseas business from English/Chinese to Chinese/English and liaising with potential business partners• Responsible for pharmaceutical packaging registration in China Food and Drug Administration (CFDA) and liaising with Guizhou CFDA officers• Involved in quality control, finding and correcting errors in the laboratory manual and improving the documents which were used for auditing and involved in external auditing• Responsible for one assistant who reported to me• 8 packages successfully passed the examination of Guizhou Food and Drug Administration; substantial progress in Japanese overseas business