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IT Quality Manager(Supervisor) 25000-30000 收藏 投递简历
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IT Quality Manager(Supervisor)

25000-30000
江苏-苏州 | 不限经验 | 不限学历
2022-12-12 更新 被浏览:
电话:0512****98200 请登录个人账号开放联系方式 登录个人
地址:苏州工业园区钟园路259号
职位描述
招聘人数:2 人 到岗时间:不限 性别要求:不限性别 婚况要求:不限婚况

This position resides in the Suzhou site and is responsible to ensure the compliance of systems in IT responsibility for Roche Diagnostics Suzhou. The compliance scope includes GxP regulated computerized systems, Site IT security contact, IT risk management, Data privacy and IT operational process for non-GxP system life cycle, primarily for Roche Diagnostics Suzhou. The incumbent will also be part of the virtual team in supporting the Global IT Quality.


?    Liaise with global IT quality and RDSZ local quality to be the owner of local IT Quality Policies (QAP), quality related operation process (SOP), tools and standards to the stakeholders (e.g. Business, Global Functions, Global Site IT)
?    Develop/maintain quality procedures along the life cycle of in-scope computerized systems
?    Keep compliance information in ITSM tool updated,, Site IT risk register and associated mitigation activities
?    Support project activities as IT Quality Assurance, in particular for local GxP IT projects
?    Support IT lifecycle processes such as change control and document management
?    Provide training related to IT systems quality and compliance
?    Support Site Business, when needed, as extension of Site Quality and Global IT Quality, for the topic of Data retention, Data Privacy & Electronic Change management process


Main  Tasks & Responsibilities:

IT quality management for IT projects
?    Act as the single point of IT quality for all projects assigned, typical tasks include managing project risks in GxP area, developing IT system validation plan, reviewing IT system validation results
?    Act as a project team member from the start of the project, to define relevant project adaptation of  IT governance processes such as PMM,CSV and CSA; Understand scope, complexity and delivery approach of the project to effectively influence the IT quality best practices used in this project
?    Support tailoring of project deliverables and the PMM paths according to the selected route, advising On the number of documents and the content material to be produced
?    Escalate nonconformance identified during project which may risk the quality of the project


Ensure that internal and external standards are met
?    Provide advice On the current standards such as PMM, documentation standards, Infrastructure Qualification, Roche CSV policy and directive, system risk assessment, data privacy, GxP assessment, test documentation and change management
?    Support RDSZ local quality team to review and approve respective IT areas within local business QMS, and stay flexible to be the extension of local quality team when the incumbent’s qualification applies
?    Act as the internal auditor, perform Internal audit based On the approved site internal audit plan
?    Provide training / support to the team members On document standards and use of templates when required
?    Act as IT quality SME for CSV related topics during ISO 13485 and cGMP audit In the quality document controller role, to ensure quality of all formal IT documents
?    Support creation/review/approval of life cycle documents using the established templates in PMM
?    Support creation of GxP related IT governance SOP following global/local templates
?    Manage changes in Service Now in the role of IT Quality



求职提醒:求职过程请勿缴纳费用,谨防诈骗!若信息不实请举报。
该公司的其他职位
会员等级
  • 生物/制药/医疗/护理
  • 股份制企业
  • 1000人以上

作为全球最大的生物技术公司,罗氏在抗肿瘤、免疫、抗感染、眼科和中枢神经系统等领域拥有一流的差异化药物。罗氏在全球体外诊断和基于组织的肿瘤诊断领域享有领导地位,同时也是糖尿病管理领域的先驱者。制药和诊断相结合带来的独特优势使罗氏成为个体化医疗的领导者,我们旨在通过个体化医疗为每一位患者提供最佳治疗方案。
  自1896年成立以来,罗氏始终致力于不断探索更好的疾病预防、诊断和治疗方案,持续为社会做出贡献。在世界卫生组织基本药物目录中,有29个罗氏开发的药品,包括用以挽救生命的抗生素、抗疟药和抗肿瘤药物。罗氏连续七年蝉联道琼斯可持续发展指数制药、生物技术和生命科学领域的领导者 。
  罗氏总部位于瑞士巴塞尔,业务遍及全球100多个国家。
  2015年,罗氏全球员工超过91,700名,研发投资93亿瑞士法郎,总销售额达481亿瑞士法郎。美国基因泰克公司(Genentech)是罗氏集团的全资子公司。此外,罗氏也是日本中外制药株式会社(Chugai)的控股方。

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