[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：熟练	电脑要求：精通
职位待遇
薪资待遇：面议	福利待遇：社保,年终奖
招聘要求

Quality Manager Assistant

Remark: Pls send us your English resume. 请提供英文简历，否则直接pass，工作语言环境为英语。这个职位首要的要求是英语口语及听力，学历要求本科以上，要求有品质工作经验，工作内容主要是涉及支持性的文职工作和QE的工作。

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.

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

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

公司信息：公司为欧资，产品为机械类和无菌产品