宜昌招聘

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 are accomplished within schedule, and OEE, scrape rate are meet the KPI. 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。


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。

Education Background: 教育背景

? Bachelor or Master Degree 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. 接受过GMP、验证、精益管理、统计的培训优先。
? Fluent in written and reading English. 流利的英语听说技能。

Main Job Tasks 主要工作任务:
? Be the process owner of appointed production line. 担任指定生产线的工艺负责人。
? Ensure the stability of process, production line and system. 保证工艺流程、生产线设备和系统运行稳定：
o Increase the stability of the equipment/systems performance by reducing variations. 通过减少变动提高生产设备和系统运行的稳定性。
o Identify best practices for work processes and make sure they are anchored in the relevant documents. 识别更优工作方法并保证其背记录到相关的文件中。
o Continuously improve corrective maintenance and preventive maintenance base on the statistical data . 依据统计数据持续改进纠正维修和预防维修工作流程。

? Optimize existing process: 优化改进现有工作流程：
o Continuously look for improvement and be seen to think out of the box on manufacturing technologies. 在生产制造技术的基础上扩大眼界和思路，持续发觉改进工艺流程的机会。
o Constantly ensure to decrease scrap and increase production efficiency from processes through implementation of Kaizen ideas and PIP projects. 通过改善项目的执行不断地提高生产效率、降低废品率。
o Implementation of changes to improve process. Handling of change requests in relation to changes.执行变更，改善工艺，处理变更（CR）。
o Lead and drive engineering activities for operational excellence.

? Trouble shooting on complex technical issues. 解决复杂的技术问题：
o Lead root-cause investigation of production issues. 主导生产问题原因调查。
o Actively engage in solving deviations. 处理偏差。
o Apply systematic problem solving tools to daily trouble shooting, drive the follow-up on the problem solving. 用系统化解决问题的方法解决问题并跟踪进展情况。

? Validation of process and equipment. 执行工艺流程和生产设备验证：
o Plan and perform validation activities, includes initiate CR, draft validation document, plan test until hand over to production successfully. 计划并实施验证活动：启动CR、撰写验证文件、计划并实施测试直到交付生产实施。
o Evaluation process periodically and maintain validation status. 定期执行工艺流程评估，维护验证状态。
o Ensure all validation activities are in compliance with GMP and NN requirements. 确保所有验证活动遵循GMP和NN要求执行。

? Set up and develop standards for processes and equipment. 建立工艺流程和设备的标准：
o Implement and develop already existing standards where available. 执行并开发现有标准。
o Create new standards where needed. 建立新标准。

? Participate in process related projects. Ensure all projects are governed and implemented according to NN PPM model.　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　 参与工艺相关项目，保证项目的管理和实施遵循NN项目管理方法。　

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.