[深圳] 欧罗巴科技有限公司 招聘 Quality engineer, manager assistant

基本信息
企业名称：欧罗巴科技有限公司
企业地址：深圳南山
公司行业：生物医药	公司规模：20人以下
公司类型：代表处	职位类型：医疗/卫生/护理/美容/保健类
职位名称：Quality engineer, manager assistant	招聘人数：2 人
职位要求
专业要求：工科类	性别要求：不限
年龄要求：不限	学历要求：本科
英语要求：不限	电脑要求：精通
职位待遇
薪资待遇：面议	福利待遇：年终奖
招聘要求

Quality Engineer （下面还有一个，工作语言为英语）
Date: 30 Oct 2014

Job description
We welcome you to work with our local team in Shenzhen China. As a quality engineer you will support the test products and systems by developing and testing specifications and methods. You will be responsible for monitoring, testing and inspecting products to make certain they meet specified standards. Tasks include product performance and lifetime testing, product failure analysis and design and process improvement. Additionally you are required to support the local development team.

Your Team:
You will work with a small team of people focusing on Quality Control at local contract manufacturers but also internally as a test engineer supporting the local development team. The team in China is responsible for daily planning, design engineering, strategic purchasing, regulatory compliance, and service operations and manufacturing. In this role you will challenged to ensure that the products manufactured externally meet EPG standards and expectations.

Your Responsibilities:
• Develops mechanical and electromechanical products by researching and testing manufacturing and assembly methods and materials; soliciting observations from operators
• Serve as a point of contact in processing, monitoring, reporting, and resolving problems and process improvements
• Designing and implementing cost-effective equipment modifications to help improve safety, reliability and throughput
• Developing a project specification with colleagues
• Discussing and solving complex problems with manufacturing departments, sub-contractors, suppliers and customers;
• Making sure a product can be made reliably and will perform consistently in specified operating environments;
• Planning and designing new production processes
• Recommending modifications following prototype test results
• Using research, analytical, conceptual and planning skills, particularly mathematical modeling and computer-aided design
• Considering the implications of issues such as cost, safety and time constraints
• working with other professionals, within and outside the engineering sector
• Confirms system and product capabilities by designing feasibility and testing methods; testing properties.
• Develops manufacturing processes by designing and modifying equipment for fabricating, building, assembling, and installing components.
• Assures system and product quality by designing testing methods; testing finished- product and system capabilities; confirming fabrication, assembly, and installation processes.
• Prepares product reports by collecting, analyzing, and summarizing information and trends.
• Provides engineering information by answering questions and requests
• Keeps equipment operational by coordinating maintenance and repair services
• Maintains system and product data base by writing computer programs and entering data.
• Completes projects by training and guiding technicians.

Qualifications:
• Engineering education background, minimum bachelor degree.
• Two year related experience
• Ability to work in a fast-paced and changing environment; flexible and quickly adaptable to changing priorities
• Highly organized and a strong work ethics
• Results oriented
• Ability to work independently with minimal supervision
• Team player
• Good communication, Chinese, English (Oral, write and aural). At least CET-6 or equivalent level, the working language is English.
• Mechanical background
• Experienced with CAD software; SolidWorks/Pro/E or equivalent
• Experience with electronics


Quality Manager Assistant
Date: 30 Oct 2014

Job description
We welcome you to work with our local team in Shenzhen China. As a Quality Manager assistant you will have an active role in supporting the local team with the daily implementation of the Quality Management System and related procedures.

Your Team:
The team in China is responsible for daily planning, design engineering, strategic purchasing, regulatory compliance, and service operations and manufacturing. You will be reporting to the local quality and regulatory manager. In this role you will be challenged to ensure that the local purchasing, manufacturing and development activities are in accordance with the requirements of documented procedures and regulatory standards.

Your Responsibilities:
• Support the local team in the implementation of QMS procedures.
• Help to establish/update/improve WI or test protocol/report
• Help for process/ quality improvement
• Assist in the establishment of design documentation
• Perform other duties assigned by Manager to support the QA/QC department
• Serve as a resource to and facilitate CAPA investigations including data analysis, root cause analysis and developing/implementing corrective action plans.
• Perform some

Qualifications:
• Scientific or engineering education background
• One year related experience
• Demonstrates good oral and written communication skills
• Strong attention to detail
• Ability to work in a fast-paced and changing environment; flexible and quickly adaptable to changing priorities
• Highly organized and a strong work ethics
• Results oriented
• Ability to work independently with minimal supervision
• Team player
• Good communication, also in English (Oral, write and aural). At least CET-6 or equivalent level, the working language is English.
• Strong interpersonal skills, including persuasion, effective communication, objectivity, assertiveness, and thoroughness
• Effective verbal and written skills
• Proactive, self-motivated and strong collaborative abilities
• Organizational and time management skills

Additional preferred (not mandatory) experience:
• Data trending experience
• Serve as a point of contact in processing, monitoring, reporting, and resolving problems and process improvements.
• Experience with Six Sigma Process Excellence tools, training and/or certification
• Knowledge of medical device regulations and standards such as ISO 13485
• Good understanding of CAPA processes including investigations, technical writing and documentation





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