医学营养高级工艺工程师

招聘人数：1 人 性别要求：不限性别 1, Responsible for department process system management, ensure all process work in approval 负责部门的工艺管理工作，确保所有的生产工艺过程均在验证批准范围内运行。2, Be responsible for technical control when trial production transferring to commercial production. According to technical formula, make related operation procedure, an d confirm the realization of process’s critical control points. 负责新产品、新技术向大生产转化过程中的工艺控制，完成相应的验证和培训；制定相关操作规程，确认过程关键控制点。3, Connected with production practice, find any possible improvement about process. 结合生产的实际要求，组织对生产过程进行持续或专项的改进。4, Well cooperate with related department, investigate, analysis, summarize an d evaluate technical deviation, environment abnormal an d finish products’ complaint. 负责工艺方面的横向沟通，完成对工艺偏差、环境异常、成品投诉进行调查、分析、总结和评价。5. Maintain an d implement the best, surest an d easiest work processes. Initiate, participate an d facilitate the continuous improvement activities on safety, quality, cost, delivery, motivation an d environment by applying DaMaWay （including LEAN principles etc）. 维护并实施***、最可靠、最简单的工作流程；应用DaMaWay（包括精益原理等），在安全、质量、成本、交付、激励和环境方面,发起、参与并推动持续改进活动。6. According to new products strategy, assistant R&D an d QA to do production trials, monitoring of production process when trial production transferring to commercial production.根据研发新产品、新技术的需要，配合研发和QA做好试生产的安排，负责新产品、新技术向大生产转化过程中的工艺控制。7. Organize continuously improvement according to production requirements, participate in new production related, propose new production line Ｏr facility an d take charge of transferring from related department. 结合生产的实际要求，组织对生产过程进行持续或专项的改进；参与与生产有关的新项目，对新生产线、新设备、新技术提出建议方案并进行接收。8. Perform new products’ validations Ｏr rational evaluation, get approval of report.完成新品的验证或评估工作，形成报告并获得批准。9. Responsible for communication with R&D an d QA, to do investigations an d evaluations for relevant deviations, including of process, environment, complaints.负责工艺方面的横向沟通，和研发及QA有效配合，完成对工艺偏差、环境异常、成品投诉进行调查、分析、总结和评价。10. Responsible for validation, internal audit, GMP, ISO22000, FSI etc. audit which department related.负责与本部门相关的验证、公司内审、GMP、ISO22000、食品安全审核等检查。11. Strictly manage the production site an d control the production process to ensure that all the products produced are qualified. Supervise the production conditions, environment hygiene, facilities to make sure that they comply with GMP/ISO Correct an d prevent deviations in production.严格生产现场管理与生产过程控制，对生产管理和操作人员及时进行相关指导，确保所有产品合格。监督生产条件、环境、卫生、设施等应符合GMP/ISO的要求。对生产操作过程的异常、偏差进行纠正与预防。12. Ensure that all the products are manufactured according to the relevant company regulation an d documents in order to guarantee the quality of the products. Issue the relevant SOPs, Production Instructions, etc. an d ensure its implementation. 确保所有产品严格根据有关文件生产，以便获得所需质量。制订有关SOP、生产操作指令等，并确保其严格实施。13. Other duties disposed by N 1 manager. N 1安排的其它工作。任职要求：1.Bachelor Ｏr above, with major on pharmaceutical Ｏr related area
学士或以上, 制药或相关专业
2.3 years related working experience of pharmaceutical/food industry with manufacturing, lean, Ｏr engineering, etc
3年以上制药或食品行业，制造、精益、或工程工作经验
3.Be familiar with ISO22000, GMP an d other correlative regulations on enteral nutrition.
熟悉ISO22000,GMP等与肠内营养相关的法规
4.Work initiatively an d can work under pressures.Easy communication, good team player.
工作主动，能承担一定的压力，良好的沟通能力和团队合作精神
5.Easy contact an d interaction with different types of persons, good managing an d coaching skills.
容易与同事相处，有管理及指导员工的能力
6.Proficient English communication skill （written an d verbal），Excellent MS office skills
良好的英语听、说、读、写能力，能够熟练使用办公软件