Shenzhen, Guangdong Sheng
1 day ago
SSMR ME Manufacturing Engineer 制造工程师
Do you want to join us in helping to fight the world's most threatening diseases and enabling access to care for more people around the world? At Siemens Healthiness, we pioneer breakthroughs in healthcare. For everyone. Everywhere.We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally.

Mission:
Perform planning of related manufacturing processes (e.g. SMT - line, Wave soldering) for printed circuit boards and complex electronic assemblies. Perform new product introduction, NPI and sample building, incoming inspection. Implementation of changes and mass production. Improve manufacturing processes for complex electronic assembly products (Cabinet, Filter plate, etc. )- Taking outstanding quality and on time delivery into account. - Work according to our quality system for medical devices.
执行计划相关的生产流程 (例如 SMT -线、波峰焊接)印刷电路板和复杂的电子组件。生产新产品导入, 样品生产,来料检验。 实施产品变更和批量生产。执行计划相关的生产流程(例如机柜组装测试)。生产新产品导入,实施产品变和批量生产。根据我们的医疗设备质量体系工作并准时交货。


Responsibilities:
Organize and perform the new product introduction as well as product changes. Prepare all relative manufacturing documents in advance. Introduce manufacturing and packaging concept as well as related documentation to production.组织和执行新产品导入以及产品的变更。提前准备所有相关生产文件。介绍生产和包装的概念以及生产相关的文档。
Ensure with Development, Industrialization as well as Manufacturing Engineering teams (China and Germany) that all relevant know-how, tools, requirements and specifications regarding production have been provided in time.确保与发展、工业化以及制造工程团队(中国和德国)的所有相关知识,工具,需求和规范及时提供给到产线。
Provide, archive all related documents for manufacturing to production self responsible. Replace documents in case of product changes. (e.g. Create Routing, Device Master Record - DMR, work instructions and descriptions, Master Data in ERP-System). 提供、归档所有相关文件对制造业生产自我负责。 替换文件的产品变化。(例如创建工作时间,设备主记录,文档管理记录,工作说明和描 述,在 erp 系统主数据)
Check the results of production according given requirements. Detect and prevent processing and manufacturing problems. Initiate and implement improvements in accordance with senior engineers. In case of ""non conformities"" suggest, initiate and follow up technical improvements in accordance with Siemens QM-System. 根据给定要求检查生产的结果。检测和防止加工和生产问题。按照高级工程师的建议对不良品发起和实施改进,按照西门子品质管理体系发起和跟踪技术改进。
Technical support for manufacturing during the product life cycle time. Align manufacturing processes also with requirements and implementations of PLM department. Technical clarification of issues regarding Product assembling.在产品生命周期的时间内对制造业技术支持。使生产过程与研发部门的需求相匹配,澄清产品装配技术的问题

Create quality inspection (first sample inspection / regular inspection) for sourcing parts and perform first sample inspection self responsible. In case of deviations, initiate counter measures in accordance with QM and SPR department. 针对采购零部件创建质量检验(首样检验/定期检查)并负责完成首样检验。在偏差的情况下,依照品质管理和采购部门的要求启动应对措施。

Responsible for introduction, coordination and communication within the complete NPI/Sample/Change process including backlog controlling. Responsible for control board and is responsible for all all internal stakeholders including risk and escalation management"负责整个 NPI/样品/变更流程的导入、协调和沟通,包括积压工作的控制。负责控制委员会,并对所有内部利益相关者负责,包括风险和升级管理
Support in validation and verification of production processes, including the complete documentation and assembly plan. Coordinate all related sub tasks to meet on time delivery.生产过程的验证和验证的支持,包括完整的文档和制造计划。协调相关任务完成准时交付。


Requirements:
1. 2 years above experience in related field e.g. PCBA or assembly manufacturing experience2. knowledge about production of electronics and complex electronic assemblies including principles of assembly and testing. 3. Knowledge of First Pass Yield, Design for manufacturing, FMEA .4. SAP Knowledge on manufacturing engineering and QM related modules (e.g. routing, BOM, Document management, SAP-EDM, Change Management)5. Knowledge and capability of MS Office and Web applications required.。6. Ability to review technical drawings and specifications (e.g. electronic components descriptions)7. Has the overview and the ability to assess the technical complexity.8. Excellent verbal and written communication in Chinese and English.9. Communication skills, Methods of organizing, cooperation 


Our global team:We are a team of 71,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what’s possible in healthcare to help improve people’s lives around the world. We aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways.
Our culture:
We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what’s possible, to improve people’s lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success.
As an equal opportunity employer, we welcome applications from individuals with disabilities.
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