(1)Assist the Department Manager to complete the establishment and daily operation of QMS. 协助部门经理完成公司QMS的建立及日常运行;
(2)Translate QMS documents, Participate in various quality activities of the company. 翻译公司的质量体系文件等,参与公司的各种质量活动.
(3)Responsible for the document control of the company's quality system documents, DHF file and purchase inspection. 负责公司质量体系文件,产品文件和进货检验的文档控制。
(4)Responsible for the development of prototype and formal material quality inspection, complete inspection records and reports. 负责研发样机及正式物料的质量检验,完成检验记录和报告。
(5)Assist in dealing with the refund and exchange of substandard products of R&D samples and formal materials. 协助处理研发 及正式物料的不合格品退换货事宜。
(6)Other duties assigned by Manager. 领导安排的其他工作。
任职要求:
(1)Bachelor degree or above, 3 years or more experience in medical device industry..
本科以上学历,三年以上医疗器械行业质量工作经验;
(2)Familiar with design tools, such as Auto-CAD, Creo etc. Good documentation skills and habits, to assist in the preparation of quality system documents.
具有良好的文档编写能力和习惯,能够协助编写质量体系文件;
(3)Good English listening and speaking ability
具有良好的英文听说能力;
(4)Good team work, communication skills and pressure resistance。
有良好的团队合作,沟通能力和抗压能力;
(5)Rules and regulations training, QA training.
接受公司规章制度培训、质量培训等。
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