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面议
苏州工业园区 | 无需经验
发布时间:2020-07-22 23:30:11 | 截止时间:2020-09-30
基本信息:
  • 其他
  • 全职
  • 若干
  • 质量部
职位描述及要求:
  • POSITION SUMMARY(职位概述)
    Engage Quality control verification activities within the plant to meet quality, service level, cost and business objectives.
    从事质量控制确认工作以达到工厂在质量,服务水平,成本和商业方面的目标。

    KEY RESPONSIBILITIES(主要职责)
    ? Responsibility of the incumbent to perform all tasks in a safe manner, keeping in mind safety awareness at all times. It is expected that the incumbent will not only practice safety on the job but will be responsible for the safety of others working in the area.
    确保自己不管是在工作中还是工作外,对自己还是他人,任何时候都具有安全意识。
    ? Implement and complete the tasks on raw material verification and release, HALB and FERT product verification, stability monitoring, customer complain investigation and validation.
    实施并完成原材料确认放行、半成品及成品确认、稳定性监控、客户投诉调查和工艺设备验证。
    ? Work on verification relative tasks in conjunction with Manufacturing, Reagent, materials and Engineering counterparts on new product introduction, material change projects.
    分别与生产部,试剂部,物料部和工程部合作,负责新产品引入,物料变更等相关确认工作。
    ? Take responsible for related data trending analysis.
    负责相关数据的汇总分析。
    Lead or participate in assigned projects and/or tasks to promote efficiency, verification and implementation of solutions and control processing to achieve product and process conformance.
    参与或领导分配的项目,以提高方案的效率,有助于生产工艺的实施。
    Provide technical guidance to other personnel and assigned teams; mentor others in the organization.
    领导团队并为成员提供技术指导。
    Performs any other task(s) as assigned, or defined in related quality procedure.
    完成其他与质量程序相关的任务。

    SKILLS AND ABILITIES(技能)
    Bachelor’s degree or above degree in Biochemistry, Biology, Medicine, or related science.
    本科或以上学历,生物化学,生物,医学等相关专业。
    Bi-lingual (English and Mandarin), with excellent interpersonal and presentation skill.
    良好的中英文沟通和表达技巧。
    Ability to interact and communicate effectively within a multidisciplinary group.
    能够有效的与多部门的人沟通。
    Logical approach to problem solving and troubleshooting.
    解决问题和排除故障的逻辑思维能力。
    Familiar with ISO 13485 and GMP.
    熟悉ISO 13485和GMP规范。

    DESIRABLE(优先条件)
    About 3 years working experience in immunoassay technologies in advance.
    具有3年免疫分析技术的工作经验优先。
    Familiar with QC tool, CI tool, Project Management and Validation.
    熟悉QC工具,持续改善工具,项目管理和验证。
    Background in laboratory experience (research, industrial or clinical).
    实验室经验(科研,工业或临床领域)。

岗位条件:
  • 本科
  • 英语 良好
  • 不限
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  • 外商独资、外企办事处
  • 制药/生物工程
  • 100-199
  • 工业园区出口加工区B区瑞浦路9号
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