We at Siemens Healthineers? are committed to helping healthcare providers globally to succeed in today’s dynamic environment. We are inspired to transform the way things are done – because we want what is best for our people, our customers and ultimately the health of mankind. While we are invested in engineering excellence – leading-edge medical technologies and services, we don’t stop there. We’re also deeply invested in our 46.000 people with the hearts of pioneers and minds of engineers, highly committed and connected in this industry. And as we strive to shape the future of healthcare, our overall success will depend on our ability to continuously reinvent ourselves.

If you are ambitious and change makes you thrive, help transform Siemens Healthineers into a learning organization:

1.Transact all product licenses needed to do business. 辦理業(yè)務(wù)所需的所有產(chǎn)品注冊證
2.Take care product-specific and general regulatory deadlines. 監(jiān)督各項產(chǎn)品的注冊時限, 整體注冊時限
3.Prepare documents and files to contact states authorities and organize business contacts, work on timely and legally correct delivery of all necessary registration material for SHD products. 準(zhǔn)備文件和檔案，以及時、合法、正確的方式遞交公司產(chǎn)品注冊所須的資料。負(fù)責(zé)聯(lián)絡(luò)相關(guān)政府機構(gòu)，聯(lián)系相關(guān)業(yè)務(wù)活動。
4.Reports process and document failures to the respective departments and handles the data update, substitution and also translation matters together with the respective dept. 向相關(guān)部門報告產(chǎn)品注冊進(jìn)程及文件不合格狀況，通過與各部門合作處理文件數(shù)據(jù)的更新、替換及翻譯等事務(wù)。
5.Works on reporting critical issues to Management. 向管理層報告緊急、危機事件
6.Support market research on planned government and competition activities. 根據(jù)政府計劃及競爭活動的安排支持市場研究.
7.Daily working with our international Regulation affairs colleagues using our existing data pool. 通過使用現(xiàn)有的資料庫與公司全球法規(guī)和注冊事務(wù)方面的同事保持日常合作。
8.Other related projects or tasks assigned by supervisor or company. 其它上級或公司指派的項目或任務(wù)。

This position may suit you best, if building learning organizations is your expertise and you have extensive experience with Top Management Learning and Leadership Development.

? At least 3 years RA experience, knowledge in PRC regulations and rules, with medical/ biological education.
? Effective communication skills both written and verbal
? Is highly computer literate with good experience in using Microsoft Office applications
? Has a thorough knowledge of Company Procedures and Policies
? Good understanding of the Financial system operated within the company
? A broad based knowledge of the products within the In-Vitro Diagnostics industry
Relevant and demonstrable knowledge of the market in which MED DX operates