招聘人数:1-2人
到岗时间:不限
年龄要求:不限
婚况要求:婚姻状况
Review batch record and release Semi- finished and final product
负责产品的批记录审核以及合格半成品/成品的放行。
Assist with QA engineer handling non-conforming issues and materials issue of incoming in-process materials.
协助质量工程师处理一些不合规的质量问题, 处理原材料和中间品的在生产过程中出现的质量问题。
Coordinate raw material issues with supplier.
与供应商联系协同处理原材料物料问题。
Designated to block nonconforming incoming material and final product.
冻结不合格的原材料,半成品及成品。
Participate in customer complaint investigation.
参与客户投诉调查。
Perform daily roving inspection on site
完成生产车间日常巡检工作。
College above degree major in Chemistry, Biology, Pharmaceutical etc.
大专以上学历,化学、生物学、药学等专业。
Familiar with ISO 13485 standard and Good Manufacturing Practice
了解ISO13485,GMP.
At least 2 years QA experience in medical or biotech related manufactory for technical degree.
至少具有2年制药、食品或医疗器械行业相关的QA工作技术经验。
Bachelor degree, fresh graduated also is accepted.
本科学历应届毕业生也可以接受。
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