西门子(深圳)磁共振有限公司

单位：西门子(深圳)磁共振有限公司　　地点：图书馆二楼报告厅　　

时间：2015-10-9 10:00　　

西门子(深圳)磁共振有限公司2016校园招聘信息

·公司简介

西门子（深圳）磁共振有限公司（SSMR）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MR（磁共振成像系统）、AX（X射线血管造影系统）以及CV（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企业。

在西门子医疗的全球战略支持下，SSMR迅速成长为除西门子MR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。

为满足全球客户对医疗产品日益增长的需求，西门子医疗在继续扩充深圳的MR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AX和CV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。

·招聘职位

(SSMR) (MR) RF R&D Engineer/射频开发工程师 (R&D)

What are my responsibilities?

-RF circuit design down to component level on MR product, including RF coils, RF power amplifier, transceiver, and other RF infrastructure;

-Perform design validation and create technical documentation, including design specification, test specification, etc.

-Work closely with internal customer to provide high quality and cost performance RF coils and components;

-Support design transfer to manufacturing;

-Support troubleshooting in the production and customer site;

What do I need to qualify for this job?

-RF design & HW engineering background, bachelor degree and above;

-Good understanding about Electromagnetic Field and microwave Theory and essential theory of Signal and System;

-Good knowledge about mixed circuit of analog and digital signal processing;

-Good knowledge for analog and RF metrology, familiarity with RF test; equipment including network analyzer, spectrum analyzer, noise analyzer, signal & waveform generator, power meter etc.;

-Knowledge for analog and RF circuit simulation, such as Spice, ADS;

-Knowledge for 3D simulation via EDA tools, such as CST, HFSS etc.

-MR product knowledge is plus, Medical device is preferred;

-Very good knowledge for the whole HW development process;

-Profound knowledge for components test and PCBA manufacturing;

-Experience of Mat lab, C++ programming is a plus;

-Experience on EMC and safety is a big plus, familiar with basic EDA tools,such as mentor, allegro, etc.

-Good communication skills and good at co-operation with people of different background and cultures.

(SSMR) (MR) Mechanical Engineer/机械工程师 (PLM)

What are my responsibilities?

-Mechanical design down to component level on MR product;

-Plan, design and perform mechanical related unit tests and integration tests;

-Collaboration on the product definition / product structure plan;

-Maintain and improvement of existing product;

-Select and cooperate with external component suppliers

-Support design transfer to the manufacturing

What do I need to qualify for this job?

-Major in Mechanical Engineering (Master degree or above)

-Familiar with NX, UG and Auto CAD etc., to create solid models and detailed drawing preferred;

-Familiar with mechanical design, sheet metal parts design and thermoplastic design;

-Familiar with machining process and thermoplastic manufacture process;

-Experienced in mechanical testing

(SSMR) (MR) Protocol develop Engineer/协议开发工程师 (R&D)

What are my responsibilities?

-Optimized MRI sequence parameters (protocol) for new software, including software upgrade or new system software

-Performance system test, which is checking the system function, such as workflow, image quality and post processing function

-Handling customer complaint regarding application, mainly for image quality

-Help sequence developer to optimize protocol for new sequence, work in progress etc.

-Test some hardware component performance, such as new coils, on image quality

-Some training to customer who buys new system or new software from SSMR, including site visiting

What do I need to qualify for this job?

-Medical university degree (Master or higher)

-Basic know-how of anatomy

-Basic know-how of MR physics and MR sequences

(SSMR) (MR) Sequence developer/序列开发工程师 (R&D)—Intern Position

What are my responsibilities?

-Research, develop and optimize on MRI sequence

-Develop and maintain MR product projects

-Generation of functional and design specifications for clinical applications derived from released requirement specification

-Investigate and solve customer complaints

-File patent applications for newly developed application techniques and subsequent authoring of scientific publications (in journals and conference contributions)

-Some training to customers, or collaborate with customer on some research topics

What do I need to qualify for this job?

-Biomedical, Physics (Master or higher)

-Basic know-how of MR physics and MR sequences

-Good communication skill (Mandarin and English)

(SSMR) (MR) Electro-Magnetic Analysis Engineer/电磁分析工程师 (R&D)

 What are my responsibilities?

-Analyzes current product/process to improve / establish the optimized working processes through R&D theoretical simulation, programming and experience.

-Under supervision to be responsible for design, fabrication, modification, and evaluation the MR component to fully support new product released on time.

-Maintain knowledge of relevant new technologies and competitor IP to maintain a technical advantage in the market

-Attend global conferences in related topics to maintain network and knowledge

-Input into the team's strategy and technology roadmap

   What do I need to qualify for this job?

-Sound Electrical / Magnetic Engineering knowledge or Material knowledge

(SSMR) (MR) Software Develop Engineer/软件开发工程师 (R&D)

 What are my responsibilities?

-Design and implement MR application software;

-Implement code with sufficient unit-test;

-Perform software integration within the whole MR system;

-Fix software bug reported during projects and product maintenance phase;

-Write and review technical document;

 What do I need to qualify for this job?

-Software Engineering, Computer Science and Engineering, Electrics and Electrical Engineering background, bachelor degree or above

-Experience in C++ or C# programing, 3+ years

-Experience in Object oriented software design

-Experience in large scale software development project

-Experience in cooperation work in team or multiple locations

-Fluent English reading and writing

-Knowledge in UML, design pattern

-Knowledge in RUP, Agile development process

-DICOM standard, Medical device knowledge is a plus

             (SSMR) (MR) Adoc Engineer/用户文档工程师 (R&D)

What are my responsibilities?

-Create User Document for medical system: The user document engineer shall understand the user document structure and contents, be responsible for the user document creation with special tools at concrete project phases.  The relevant actions shall be synchronized in SSMR internally, user document service supplier and HQMR.

-Control and manage Product Document. The user document engineer shall be responsible for controlling and management of user document according to project requirements. The information for user document shall be managed to collect, transfer, verify, and release. The relevant actions shall be synchronized in SSMR internally, user document service supplier and HQMR.Perform software integration within the whole MR system;

-Manage Foreign Language Version. The foreign language support shall be defined in project. The foreign language version shall be created, reviewed and verified based on the original (mostly English) version. The user document engineer shall be to manage the whole actions. The relevant actions shall be synchronized in SSMR internally, user document service supplier and HQMR Write and review technical document;

-Coordinate and cooperate with external suppliers. This is one part of creation of user document. The relevant information, e.g., the layout, content, project time line shall be transferred to external suppliers and synchronized, so as to match the project time line.   The relevant actions shall be synchronized in SSMR internally, user document service supplier and HQMR.

-Manage UI translation and verification. The user document engineer shall be responsible for the management of UI translation and verification and delivery to product according to project requirements. The relevant actions shall be synchronized in SSMR internally, user document service supplier and HQMR.

-Translate and verify non-SSMR projects. The user document engineer shall be able to provide service for the project not in SSMR by means of local supplier of A&D. The relevant actions shall be synchronizedwith HQMR and A&D.

-Manage online help. The user document engineer shall be responsible for management of editing, translating and verifying online help.

 What do I need to qualify for this job?

-bachelor degree

-major in Biomedical engineering or mechanical engineering orelectronica engineering

(SSMR) (MR) Equipment Engineer/设备工程师 (SCM)

 What are my responsibilities?

-Manage, maintain and repair equipment and facility effectively, new equipment and facility installation, which meet the needs of production plan. And develop new equipment to improve equipment efficiency                            

-Implementing maintenance according to the maintenance plan and instruction to keep the good efficient.                                                

-Evaluate the measurement equipment's calibration period according to production frequency. Giving advice to use proper measurement equipment when new or revised process is created.                  

-Manage and replace spare part of the equipment to keep low and acceptable inventory         

-Providing training to maintenance technician to improve technology ability.        

       What do I need to qualify for this job?

-Engineering background

-Equipment maintenance, calibration and repair skills, Trouble shutting and IT

-Mechanical and electrical knowledge

(SSMR) (MR) RF Process Engineer/射频工艺工程师 (SCM)

               What are my responsibilities?

-Technological support the RF product 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 RF, electronic or Automation.

-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) 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?

-Bachelor degree、major in Mechanical is preferred

-Perfect English

-Product knowledge

-Domestic and International Pressure Vessel Regulations

(SSMR) (AX) Software Develop Engineer/软件开发工程师 (R&D)

What are my responsibilities?

-Develop software under constrains of the related legal, regulatory, and normative requirements;

-Plan and estimate resource of module and unit development incl. test activities and documentation;

-Concept design and specify low level software architecture, aligned with the system software architecture;

-Create and update the functional specification of the software components;

-Integrates modules on unit level and performs unit tests;

-Prepare of supply chain of software components and tools；

-Support QIB by solving field issues；

-Perform/create design transfer；

-Work on changes incl. Documentation and tests.

 What do I need to qualify for this job?

-A Master’s degree in computer engineering or science or related discipline and relevant experience in software design.

-Strong understanding of software development basics like C, C++, C#, xml, OOD/OOP experience

-Experience with software development CASE (Computer Aided/Assisted Software Engineering) tools like IBM Rational rose etc.

-Knowledge of control software development for embedded system and understanding embedded system architectures and communication protocols

-Experience and knowledge of TCP/IP, CAN and Profaned

-Experience of Software development of motion control is a plus

-Experience in medical engineering or clinical use of medical devices, preferably in the range of X-ray, Angiography or Cardiology systems is a plus

-Fluency in English and good in communication skill

-International travel is required.

-Be available for internship before graduation.

(SSMR) (AX) Strategic Process Specialist/战略流程改进专员 (SCM)

 What are my responsibilities?

-Analyze processes and derive and implement optimization measures;

-SCM Supply Chain Controlling and profound data analysis;

-Drive and implement continuous improvement (cost down and quality up) and development of the LEAN Supply Chain;

-Visualize processes, methods, KPIs, etc. within SCM;

-Identify and implement new concepts, ideas and technologies;

-Develop and implement worldwide logistical concepts

-Organize and moderate workshops with proceeds owners to generate improvements potentials

 What do I need to qualify for this job?

-Master degree and major in business admin or technical /engineering;

-Very good knowledge of process analysis and improvements, LEAN methods, etc.;

-Experience in project management;

-Excellent communication skills including, presentation. moderation, persuasion, listening and asserting;

-Excellent English, both in writing and speaking;

-Customer focus, drive, strategic thinking, change management, analytical skills, team player;

-IT Skills with MS office, SAP, specific SCM Tools;

-Be available for internship before graduation.

      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-集团-专业

      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