莆田招聘

Education Background: 教育背景
· Bachelor Degree and above in manufacturing engineering or similar education background. 制造工程或相关学科领域大学本科及以上学历。
· Education/training of GMP regulation, validation, LEAN and statistics is preferable. 最好接受过GMP、验证、精益管理、统计的培训。
· Fluent in written and reading English. 流利的英语听说技能。
Professional Experience专业经验:
· Minim 4-6 years of relevant working experience. 至少4-6年相关工作经验。
· Experience in automation and mechanical areas. 机械、自动化领域工作经验。
· Experience of working in a production environment with highly automated machines. 在高度自动化设备生产环境的工作经验。
· Experience of GMP/ISO 9001/ISO 13485 regulated production, validation and change procedures. GMP、ISO9001、ISO13485标准化要求的生产、验证、变更管理流程的工作经验。
Key areas of responsibility 主要工作职责:
Process engineer is responsible for compliance of daily production activities that to ensure quality and efficiency of production. Work according to GMP, GDP and SOP. Ensure NC, CR, PSE, QAP, validation, etc. are accomplished within schedule, and OEE, scrape rate are meet the KPI.
In project, process engineer is responsible for technical issue, such as process design， risk assessment, validation activity to ensure quality and compliance. ensure project activity are accomplished within project schedule 工艺工程师的职责是保证日常生产活动合规，保证生产高质、高效。遵循GMP、GDP和SOP执行工作，确保NC、CR、PSE、QAP、验证等工作按计划完成；确保OEE、废品率等KPI指标达标。
在项目期间，工艺工程师负责技术问题如工艺设计，风险评估，验证活动符合质量及合规要求，确保项目活动按时完成。
Main Job Tasks 主要工作任务:
· Be the owner of appointed production machine/equipment. 担当指定生产设备的负责人。
· All actions with deadline should be finished on time, that include QAP, NC, NC3, CR, CR6, PSE, VSS, and validation document etc. 按时完成QAP、NC、NC3、CR、CR6、PSE、VSS, 及验证文件等工作任务。
· Set up metrology specification and ensure calibration meet MPE requirement. Execute machine software backup verification, machine test relevant to investigation or validation. 建立测量说明书并校准设备，以确保符合最大允许误差的要求。执行验证相关设备软件备份检查和设备测试。
· Execute process/equipment validation 进行工艺/设备验证。
· Periodically review logbook according to requirement. 按照规定定期检查日志文件。
· Update and archive all relevant documentation within in deadline after validation is finished. 验证完成之后，在规定的时间内完成相关文件更新和存档。
· Execute machine improvement when machine have down time, high scrap rate occur, and quality issue in the long time run. 当发生设备停机、废品率升高、长期存在质量问题时，进行设备改进工作。
· As process owner is responsible for handling compliance issue and all kinds of audits as well as relevant findings action. 处理合规问题和应对审计，对所有发现点采取行动。
· Use SPS problem solving method for troubleshooting. 运用系统解决问题的方法解决问题。
· Handle all reported quality incidents and close them on time. 按时处理并解决质量事件。
· Daily monitor product scrap rate and making relevant action plan. 监控产品废品率并采取相关行动。
Communication with DMD or other stockholder to ensure technical solution and project quality 和DMD或其他相关方沟通进行问题解决，确保项目质量。
职能类别：
产品工艺/制程工程师
关键字：
PE工艺工程师产线导入

诺和诺德在中国
诺和诺德是中国市场的领导者，一直以改变为己任。诺和诺德（中国）制药有限公司于1994年成立，二十几年来业务一直保持强劲增长。公司总部设在北京，产品和服务遍及全国所有省、直辖市及中国港澳台地区。截至2017年底，诺和诺德在华员工总数4329人。诺和诺德是在中国建立研发中心的生物制药公司。位于北京的研发中心是诺和诺德全球研发体系的组成部分，致力于与总部合作研发新产品及新生产工艺。诺和诺德在中国的生产厂位于天津，是公司的国际化战略生产基地。公司对工厂提供了大量的资金投入和技术支持，向全球以及中国市场供应产品。诺和诺德在中国的不断发展反映了公司对中国市场的承诺。

Novo Nordisk in China
As the leader in the Chinese market, Novo Nordisk has always been committed to Changing.
Founded in 1994 and headquartered in Beijing, Novo Nordisk’s presence in China has been growing for more than 20 years.Headquartered in Beijing, providing products and services across mainland China as well as Hong Kong, Macau and Taiwan of China. As of the end of 2017, Novo Nordisk employed over 4,329 employees in China.