常州招聘

职位概要：负责制造技术工作，以确保制造工艺和方法满足生产的需要和客户的要求。针对涉及材料、工艺、机械加工和模具的生产,样品生产等问题，负责制定解决方案及实施。通过开发新流程，协助设计部门加工新产品，控制过程质量来支持新产品项目的开发，或从美国转移产品和过程到常州工厂。通过现场支持和故障排除技术来加强对生产订单的支持。

基本职责：

· 工厂制造工艺制度和程序的开发，培训和实施监督

· 生产设备选型和试运行，设备能力研究，改善和提高， 制定各过程的产能标准

· 制造过程中相关设备的编程和程序调整

· 设计和可生产性分析

· 领导创建DMR

· 参加公司的管理评审

· 处理相应的COGS、BOM，制定生产流程及质量控制计划。

· 根据客户产品的要求确定是否需要进行夹具设计，如果需要，进行夹具设计和验证

· 制定标准的生产工时，确定生产程序和时间、编程、刀具及夹具成本，按照报价流程提供产品的报价（价格，交货期等）支持

· 车间生产过程中有关工艺，夹具，测量，质量等方面的支持

· 为概念、设计、样件和首件产品的生产流程提供技术支持，以保证最佳可生产性的产品投入生产，其中包括审查设计和批准设计变更、处理可生产性问题

· 对正在进行的工程项目提供项目管理跟踪和编程支持

· 参与过程认证和产品认证

· 参与过程更改

· 主导风险分析

· 供应商选择支持

· 样件开发支持

· 作为客户与供应商之间的连接桥梁，沟通，解决报价，生产，质量等方面问题，参与生产/采购决策

教育和经验：大专毕业后两年；本科学历，或在机械制造行业同等的经验。有管理、领导经验者优先。要求有编程经验。

技能：

· 必须具备生产计划技术的知识，能够管理资源，以满足客户的交货要求。

· 熟练操作CAD, Office等计算机软件；

· 了解并有应用精益生产，团队管理，5S, 6 sigma,等工具的经验；

· 有医疗器械制造厂工作经验，ISO13485质量体系认证经验者优先；

• 英语4级以上，书面英语熟练。

身体要求和工作环境：这里提到的身体要求和工作环境的特点是具有工作代表性的。

· 身体要求：在履行职责的时候，员工会偶尔需要站立；走路；就坐；用双手来处理、感觉或操作物体、工具;用手和手臂够物;爬上楼梯;平衡;弯腰、跪地、躺卧或爬;说话或倾听；品尝或闻嗅。员工必须偶尔升降及/或移动25磅重物。工作要求的具体能力包括近观、远视、辨色、环视、深度知觉以及调整工作重点的能力。

· 工作环境：工作在办公室环境里。工作环境中的噪音水平中等。

SUMMARY OF POSITION: Responsible for manufacturing engineering work. Ensure technique and methods to meet production and customers’ demand. Responsible for setting up solution and implementing projects related to materials, techniques, machining, mould and sampling, etc. Assist designing new products’ machining and control process quality to support new products projects’ development or products and process transferring from U.S. to Changzhou facility. Improve to support work order through site supports and exception handles.

ESSENTIAL FUNCTIONS:

· Establishes manufacture technique system and processes later with training and supervising implementation;

· Selection of equipment, trial running, research and improve equipment capacity. Sets up capacity standards of each process;

· Programming and adjustment of related equipments for each manufacturing process;

· Design and analyze producibility;

· Leads to establish DMR;

· Participates company’s management review;

· Handles with related COGS and BOM. Sets production process and quality control plan;

· Confirm to design and validate fixture according to customers’ demand;

· Establishes standard work hours. Ensure production process with time, program, costs of tools and fixtures. Supports quotation (price and delivery time, etc.) based on quotation process;

· Supports on techniques, fixture, measuring and quality in workshop;

· Supports technology for conception, design, sample and first article’s production process to ensure best producible products invested into production including examination design, change design and handling with producibility;

· Project management following up and programming supports on on-going projects;

· Participate in process validation and products validation;

· Participate in process change;

· Leads risk analysis;

· Suppliers’ selection supports;

· Samples’ development and supports;

· Communicates to solve problems about quotation, production, quality, etc. as connection between customer and supplier. Participates in production and purchase decision.

Education/Training/Experience Required:

· Bachelor's level degree in a related scientific or business field is preferred. 2 years of work experiences after college graduated.

· Knows programming.

· Has work experiences in medical manufacturing and quality system authentication is preferred.

SKILLS:

· Good knowledge in production plan technology and resource management to meet customers requirements;

· Familiar to operate CAD, Office and so on computer softwares;Comply with all of Paragon’s Quality System Regulations.

· Understand and apply LEAN, team management, 5S, 6 Sigma tools, etc.

· Well English writing and communication.

PHYSICAL DEMANDS AND WORK ENVIRONMENT: The physical demands and work environment characteristics described here are representative of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

§ Physical demands: While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to handle or feel objects, tools, or controls; reach with hands and arms; climb stairs; balance; stoop, kneel, crouch, or crawl; talk or hear; taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.

§ Work environment: Work performed in an office environment. The noise level in the work environment is usually moderate.

派瑞格集团位于世界外科医疗的“首都”-美国沃索，是首选的、可提供世界一流水平系统方案的“交钥匙”供应商。派瑞格集团自1991年成立以来，在美国、欧洲和亚洲创建了卓越的战略中心，工厂分布在美洲和亚洲，长期为世界顶尖的医疗器械生产商配套，同时也为中国国内顶尖的医疗器械生产商服务。设在美国的“全球设计中心”将服务从专业制造延伸到了客户的产品研发和样品试制，通过独特的质量管理体系，派瑞格承诺给世界范围的医疗器械行业的OEM商提供创新的、快速响应的系统方案。
派瑞格医疗器械（常州）有限公司创建于2007年5月，投资总额1850万美元，是美国派瑞格医疗国际公司在亚洲投资的全资美资公司，是派瑞格集团亚太区重要的出口生产基地。公司给全球一流的医疗器械公司专业生产符合不同国家法律法规要求的一类骨科医疗器械，器械盒和托盘，三类6846植入材料和人工器官的制造等，并可设计并销售自产产品。
我们的远景：成为全球外科手术市场上产品和成套器械管理方案的首选供应商。
我们的使命：通过设计和提供高精密的医疗器械产品，高效及时交付系统，试验和植入器件来服务于全球外科手术器械市场。
我们的质量方针：第一次就把事情做对。
更多企业信息，请关注我们的企业网站：http://www.paragonmedical.com