• 3-4年经验
  • 本科
  • 招若干人
  • 03-06 发布

职位描述

What are my responsibilities? Project/product : Ensure project management and process control complying with internal regulation, ensure products' compliance with quality requirements. Support and consult for project and process quality control. Join the reviews for the decisions of milestones. Monitor the product regulatory compliance. Tasks: Assist Quality manager to implement Quality Management System in design and manufacturing process. Familiar with process who can interprete and provide consultant on process implementation. Provide the solution for process issue during development phase to make sure process compliance. Work closely with project team and participate in the review and evaluation on relevant documentation coming from different stage of PEP. Monitor key quality process implemented on specific products who is responsible for such as complaint handling process, engineering change process, reportable MDR process, risk management process, and CAPA process, etc. Monitor manufacturing quality, initiate data analysis and corrective & preventive actions if necessary. Support internal audit and external audit. Reporting and escalation any deficiencies, do the statistics for tracking the product KPIs who is responsible for. Responsible for process optimization and quality template optimization related to project control and process control. Act as quality contact window required in the quality agreement with customer. Act as an independent quality function to review development and manufacturing documents. What do I need to qualify for this position? Experience with project quality management and process quality control and supplier quality control Experience with quality control for new product development project from design concept(D1)to mass production release (D4) Strong knowledge for ISO13485, MDD and 21CFR Part 820, ect. Bachelor above, medical device product knowledge Good English 3 - 5 years experience on medical device field 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 职能类别: 可靠度工程师 其他

联系方式

公司信息

上海西门子医疗器械有限公司(http://www.healthcare.siemens.com.cn/about-us-cn/healthcare-development-ssme-cn)成立于1992年,是西门子(中国)有限公司下属的独资公司。目前公司致力于计算机断层扫描诊断设备(CT)、X光机诊断设备、及其零部件的研发生产。相关客户服务也是我们业务的重要组成部分。公司并参与Soarian MedSuite 的全球研发及在中国的项目实施。公司被上海市政府授予高新技术企业称号。 上海西门子医疗器械有限公司不仅是西门子供应全球市场的医疗影像设备制造基地,而且是西门子医疗影像设备和医疗软件的研发中心之一。公司拥有800多名员工,其中研发人员超过270人。 上海西门子医疗器械有限公司位于上海国际医学园区(周祝公路278号),占地面积10万平方米,其中各类研发及生产区域占地超过35000平方,总投资超过3亿多人民币,是西门子医疗业务领域在亚太地区最大的研发和制造中心,也是目前上海最大的医疗器械研发生产高科技企业之一。 近几年来,公司发展尤为迅速。 CT业务部门成功研发制造了双层螺旋CT SOMATOM Spirit,以及6层16层螺旋CT SOMATOM Emotion系列。X光机部门则成功地向市场推出了中国热销的X射线拍片系统Aristos VX Plus等优质产品。 公司的客户服务部门,提供培训,区域技术支持及各类零备件的物流服务。 公司的医疗软件部门致力于研发和实施西门子全球化和本地化的Soarian MedSuite产品 公司将继续加大研发力度,为市场提供更多高品质的医疗设备和医疗软件,为健康水准的普遍提高作出积极贡献。 公司地址:上海市浦东新区周祝公路278号 邮  编:201318 公司网站:http://www.healthcare.siemens.com.cn/about-us-cn/healthcare-development-ssme-cn 公司邮箱:recruitment_healthcare@siemens.com

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