日日噜夜夜草|一级黄色录像高清版|调教白富美加勒比久久|亚洲欧洲精品婷婷|日韩综合无码色色|日韩精品一区妖精视频|亚洲无码中文字幕hd|99亚洲思思丝袜|手机看片国产精品大胆亚洲|成人无码视频一区二区在线播放

2.Project follow-up and data collection: Responsible for collection of the required technical dossiers from India team for new filing, renewal filing, variation filing, and responses to CDE query, etc.

3.Translation: Responsible for translation (English to Chinese) of received documents for various submission.

4.Documentation and submission: Compile application dossiers as per China regulations & guidance, and complete the submission as per timeline. 5.Necessary activities after initial submission: To follow up the progress of various filings and carry out necessary activities including coastal testing, answer the questions from agency timely, arrange discussion/assessment on the deficiency letter, prepare the query response for submission till final approval obtained. 6.Regulatory insight: Responsible for sharing and communication with India RA team about updated NMPA/CDE/CFDI etc. regulations and guidelines. 7.Communication with authorities: Responsible for communication with the authorities including but not limit to NMPA, CDE, NIFDC, port IDC, etc., so as to smooth the registration/coastal testing progress.

8.Others: Finish the other RA related work and BD supports sometimes for the Product and regulatory research as per assignment.

任職要求：

1. 本科或本科以上藥學(xué)相關(guān)專(zhuān)業(yè)畢業(yè)；具有良好的英語(yǔ)閱讀和寫(xiě)作能力以及比較流利的口語(yǔ)。

2. 具有藥品注冊(cè)申報(bào)資料的實(shí)際翻譯（英譯中），整理和申報(bào)遞交經(jīng)驗(yàn)；

3. 具有2年或2年以上藥品注冊(cè)申報(bào)相關(guān)工作經(jīng)驗(yàn)，尤其具有進(jìn)口仿制藥（制劑或原料藥）的申報(bào)注冊(cè)和再注冊(cè)經(jīng)驗(yàn)予以優(yōu)先考慮；

4. 熟悉《藥品注冊(cè)管理辦法》及藥品注冊(cè)相關(guān)的最新法規(guī)與指南，熟悉進(jìn)口/國(guó)產(chǎn)藥品注冊(cè)申報(bào)與注冊(cè)檢驗(yàn)流程；

5. 具有與藥品注冊(cè)相關(guān)各法規(guī)部門(mén)溝通的能力，包括但不限于國(guó)家局，省局，藥審中心，口岸藥檢所等；

6. 具有藥品注冊(cè)信息檢索和分析調(diào)研能力；