西门子（深圳）磁共振有限公司（厂厂惭搁）于2002年植根中国，是西门子医疗的独资子公司。公司位于深圳高新技术园区，占地面积超过四万平方米。业务范围涵盖惭搁（磁共振成像系统）、础齿（齿射线血管造影系统）以及颁痴（医疗器械零部件），是一家集研发、生产、物流、市场、客户服务于一体的高新技术公司。
在西门子医疗的全球战略支持下，厂厂惭搁迅速成长为除西门子惭搁事业部德国总部以外的最大研发及生产中心和西门子磁共振事业部同时拥有磁共振系统整机研发和生产能力的全球基地。&苍产蝉辫;
为满足全球客户对医疗产物日益增长的需求，西门子医疗在继续扩充深圳的惭搁研发和生产规模的同时，于2012年伊始在西门子磁共振园相继建立础齿和颁痴事业部的研发生产基地，树立了西门子医疗产业立足深圳、辐射全球的一块重要里程碑。
(SSMR) (MR) Process Engineer/工艺工程师(SCM)
What are my responsibilities?
Technological support the Superconducting Magnet production, finish the related assembly and process monitor according to our quality system and product introduction plans for medical devices.
Steering, controlling and coaching the definition, development and implementation of production process
Transferring design from PLM to production (New project and change request)
Implementing new production technologies regarding PE
Developing and maintaining production documentation (DMR、Master plan、FMEA etc.)
Developing tooling、equipment and new technology including documentation and validation.
What do I need to qualify for this job?
Master degree, majored in Mechanical or mechatronic.
The basic understanding on MR system will be better. Have some software knowledge is preferred
Fast learner and good communication skill
Good English in both speaking and writing
(SSMR) (MR) Regulatory Affair Specialist/法规事务专员 (SF)
What are my responsibilities?
Support the business by consult super conduct magnet's manufacture, supplier development and pressure vessel certification in compliance with global Pressure Vessel regulations.
Coordinate and influence activities towards 3rd parties
Incorporate the results into quality report
Development, implementation and documentation of a consistent quality management system based on pressure vessel regulatory and quality related requirements and in alignment with the Siemens process framework.
Ensure implementation and controlling of quality gates and preventive quality tools to gain a sustainable higher quality of pressure vessel manufacturing. Initiate continuous improvement with employee support. If necessary, use authority to refuse development, production, shipping and acceptance release. Incorporate the results into quality report.
Regular internal assessments based on the mandatory elements of Siemens quality management guidelines. Direct report to the RA Manager with recommendation of improvement actions
Ensure corporate compliance concerning product safety.
Check whether SSMR quality regulations are compliance with the standards, regulations and Siemens MED Qtrs.
Performed the audits as planed to check whether the SSMR quality regulations are followed effectively
Work together with process owner for the CAPA
Verify the CAPA for the non-compliance findings.
What do I need to qualify for this job?
&苍产蝉辫;欢迎有兴趣同学投递简历。
电邮：ssmr-Campus_Recruitment.healthcare@siemens.com
简历命名格式：职位名称-姓名-学校-专业
&苍产蝉辫;&苍产蝉辫;&苍产蝉辫;&苍产蝉辫;&苍产蝉辫;工作地点：中国深圳高新区中区高新中二道32号西门子磁共振园
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