(SHD)西门子医学诊断产品（上海）有限公司 & RA Specialist法规注册专员 & 北京(69036)(职位编号：69036)
西门子医学诊断产品（上海）有限公司(SHD)
- 公司行业：医疗设备/器械
职位信息
- 发布日期：2012-08-08
- 工作地点：北京
- 招聘人数：若干
- 工作经验：三年以上
- 职位类别：医疗器械注册 知识产权/专利顾问/专员
职位描述
Mission
- Support RA Manager in all activities. Fast and efficient registration and promotion of responsible product lines (Instruments and reagents) to be sold in China. 支持法规经理的所有工作，快速和高效的完成所负责产品线计划在中国销售产品（仪器和试剂）的注册及上市工作。
- Transact all product licenses needed to do business. 办理业务所需的所有产品注册证
- Take care product-specific and general regulatory deadlines. 监督各项产品的注册时限, 整体注册时限
- 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. 准备文件和档案，以及时、合法、正确的方式递交公司产品注册所须的资料。负责联络相关政府机构，联系相关业务活动。
- Reports process and document failures to the respective departments and handles the data update, substitution and also translation matters together with the respective dept. 向相关部门报告产品注册进程及文件不合格状况，通过与各部门合作处理文件数据的更新、替换及翻译等事务。
- Works on reporting critical issues to Management. 向管理层报告紧急、危机事件
- Support market research on planned government and competition activities. 根据政府计划及竞争活动的安排支持市场研究.
- Daily working with our international Regulation and Registration colleagues using our existing data pool. 通过使用现有的资料库与公司全球法规和注册事务方面的同事保持日常合作。
- Other related projects or tasks assigned by supervisor or company. 其它上级或公司指派的项目或任务。
Qualifications
- At least 3 years RA experience, knowledge in PRC regulations and rules, with medical/ biological background 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
提醒：
点击“西门子专属申请 ”，您将会进入西门子专属招聘系统，进入系统后您可以在页面右上方的下拉菜单，选择简体中文页面，并请遵循下面的规则设置您的系统密码。
密码设置规则：密码长度必须在8个字符以上，并且必须包含英文大写字母，小写字母和数字。例如：Ab123456。
- Support RA Manager in all activities. Fast and efficient registration and promotion of responsible product lines (Instruments and reagents) to be sold in China. 支持法规经理的所有工作，快速和高效的完成所负责产品线计划在中国销售产品（仪器和试剂）的注册及上市工作。
- Transact all product licenses needed to do business. 办理业务所需的所有产品注册证
- Take care product-specific and general regulatory deadlines. 监督各项产品的注册时限, 整体注册时限
- 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. 准备文件和档案，以及时、合法、正确的方式递交公司产品注册所须的资料。负责联络相关政府机构，联系相关业务活动。
- Reports process and document failures to the respective departments and handles the data update, substitution and also translation matters together with the respective dept. 向相关部门报告产品注册进程及文件不合格状况，通过与各部门合作处理文件数据的更新、替换及翻译等事务。
- Works on reporting critical issues to Management. 向管理层报告紧急、危机事件
- Support market research on planned government and competition activities. 根据政府计划及竞争活动的安排支持市场研究.
- Daily working with our international Regulation and Registration colleagues using our existing data pool. 通过使用现有的资料库与公司全球法规和注册事务方面的同事保持日常合作。
- Other related projects or tasks assigned by supervisor or company. 其它上级或公司指派的项目或任务。
Qualifications
- At least 3 years RA experience, knowledge in PRC regulations and rules, with medical/ biological background 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
提醒：
点击“
密码设置规则：密码长度必须在8个字符以上，并且必须包含英文大写字母，小写字母和数字。例如：Ab123456。
公司介绍
西门子医学诊断，作为临床诊断行业中的领导者，承诺为医护人员提供疾病诊断、治疗和监控所需的关键信息。我们不仅提供优质、范围广泛的产品线组合，包括整合生化，免疫分析，常规生化，自动化，血球，凝血，微生物，糖尿病，尿液分析，血气监测以及分子生物学检测，同时还提供丰富多样的检测菜单及IT解决方案，配合高响应的客户服务，为您优化实验室工作流程、提高操作管理效率并改善患者护理效果提供最有效的帮助。