- Responsible for submission of applications to China regulatory authorities. - Coordination with CFDA/other regulatory authorities related to all activities (submission, GMP audit, audit response submission and compliance, renewals etc…). - Responsible for verification of Chinese pharmacopeial compliance of specifications/requirements etc... - Should be able to prepare process flow chart, collinear assessments etc… for the products. - Should have knowledge on manufacturing/packing process. - Responsible for coordination of External trainings related to Chinese regulatory. - Responsible to coordination with Site regulatory, production, administration, QC etc.. teams to ensure/collect the required information/documents etc.. - Responsible to ensure the Chinese language terminologies/requirements for documents aligned for Chinese regulatory. -負責向中國監(jiān)管機構(gòu)提交申請。 -協(xié)調(diào)與CFDA/其他監(jiān)管機構(gòu)所有活動（提交、GMP審計、審計回復提交和合規(guī)、續(xù)期等） -負責確認中國藥典規(guī)范/要求等的合規(guī)性等 -應能夠為產(chǎn)品準備工藝流程圖、共線評估等。 -應了解生產(chǎn)/包裝工藝。 -負責協(xié)調(diào)與中國監(jiān)管相關的外部培訓。 -負責協(xié)調(diào)現(xiàn)場合規(guī)、生產(chǎn)、行政、質(zhì)量控制等團隊，確保/收集所需的信息/文件等。 -負責確保文件的中文術(shù)語/要求符合中國監(jiān)管要求。