Quality Technician

Johnson & Johnson

4.2

(92)

Shanghai, China

Why you should apply for a job to Johnson & Johnson:

  • Ranked as one of the Best Companies for Women in 2020
  • 4.2/5 in overall job satisfaction
  • 4.2/5 in supportive management
  • 71% say women are treated fairly and equally to men
  • 88% would recommend this company to other women
  • 85% say the CEO supports gender diversity
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Global parental leave for all new parents (maternal, paternal, adoptive or surrogacy-assisted).
  • Global exercise reimbursement.
  • Two weeks off (one of them fully paid) for volunteer work.
  • #2406184998W

    Position summary

    APTIV & CDR to perform accounts activation, deactivation, role and security group maintenance for all site users and other business related to J&J associates.

    作为工厂ADAPTIV和CDR系统管理员对所有工厂员工和其他有关联业务的强生员工进行账户的激活、注销,用户权限和安全组的维护。

    • As DRB Coordinator, support site CAPA lead to schedule DRB meeting, invite DRB attendees, facilitate the data collection and analysis from quality sub-system owners, track the progress of DRA through collaboration with DRA owners and support to maintain DRB related documentation.

    作为DRB协调员,支持工厂CAPA负责人进行DRB会议的计划安排,邀请DRB参与人员,协调质量子系统负责人进行数据收集和分析,和DRA负责人协作进行DRA的进展追踪,并支持维护DRB相关记录。

    • As site NC Coordinator, assist site NC lead to facilitate the NC process including the NC investigation, action implementation, and NC approval & Closure.

    作为工厂不合格协调员,协助工厂不合格负责人以推进不合格过程包括不合格调查,行动执行以及不合格批准和关闭。

    • Work as Site Record Coordinator to support site Record Manager to manage the process of Document Control & Record Control under Ethicon Minhang Quality Management System.

    作为工厂记录协调员协助工厂记录经理以管理爱惜康闵行质量管理系统下的文档控制和记录控制流程。

    • Participate in External/Internal audit related activities.

    参与外部/内部审核相关活动。

    • Support in quality related improvement projects.

    支持质量相关改进项目。

    • Responsible for communicating business related issues or opportunities to next management level

    负责将业务相关问题或机会传达给下一级管理层。

    • For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable

    对于那些监督或管理员工的人员,如适用,负责确保下属遵循与健康,安全和环境实践相关的所有公司指南,以及所有需要的资源都是可用的,且状况良好。

    • Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.

    负责确保个人和公司遵守联邦、州、地方和公司的所有法规、政策和程序。

    • Performs other duties assigned as needed.

    执行其他必要的职责。

    Qualifications

    章节 3 :经验和教育

    • University/Bachelor's Degree or Equivalent.

    大学本科学历或同等学历。

    • Minimum 2 years of experience in Quality function, in Medical Devices or Pharmaceutical industry.

    至少有2年在医疗器械或医药行业质量部门的经验。

    章节 4: 要求的知识,技能,能力,认证 / 许可证和附属。

    • Detailed knowledge of medical device regulatory requirement such as ISO13485 and China GMP is necessary.

    具有医疗器械法规要求的具体知识,比如ISO13485 和China GMP是必要的。

    • Must be able to communicate effectively in both English and Chinese.

    必须能有效地进行中英文沟通。

    • Ability to work cooperatively with coworkers.

    能与同事合作的能力。

    • Ability to use Microsoft office tool.

    能使用微软工具的能力。

    • Demonstrate a strong Quality and Compliance mindset.

    具有强烈的质量与合规意识

    Why you should apply for a job to Johnson & Johnson:

  • Ranked as one of the Best Companies for Women in 2020
  • 4.2/5 in overall job satisfaction
  • 4.2/5 in supportive management
  • 71% say women are treated fairly and equally to men
  • 88% would recommend this company to other women
  • 85% say the CEO supports gender diversity
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Global parental leave for all new parents (maternal, paternal, adoptive or surrogacy-assisted).
  • Global exercise reimbursement.
  • Two weeks off (one of them fully paid) for volunteer work.