医疗器械生产主管（需倒班）社

面议

无锡市4年及以上

发布时间：2023-09-06

职位描述

1.To organize, coordinate, supervise the production in CR, in a way to optimize the use of resources, improve efficiency, achieve the company mission and goals to ensure a short and long-term performance in terms of cost, quality, delivery speed, reliability and flexibility.
组织、协调和监管洁净室的生产，保证人力/材料利用的***化，提高工作效率，以确保公司在成本、品质、交货期、可靠性、灵活性等方面具体措施的实施。
2.根据公司内各项要求实施生产，执行ISO13485/GMP等有关的方针政策,确保产品的高质量。
Organize production according to company rules; ensure product superiority through 100% compliance of ISO13485/GMP, etc. requirements.
3.对生产操作过程的异常、偏差进行纠正与预防。
Implement and follow up the corrective and preventive actions to the deviations.
4.参与制订有关SOP、生产操作指令等，并确保其严格实施。
Participate the relevant SOPs, Production Instructions, etc. development and ensure a strict implementation.
5.Keep closely cooperation with QA, maintenance and planning to implement production schedule on time in full, ensure the related information communicated with stakeholders properly including of completing documentation in time.
与QA、维修、计划等密切配合，及时足量地完成生产计划任务，并保证生产信息准确传递与反馈，及时完成生产记录的收集和审核。
6.组织与推动生产过程中的问题解决以确保生产任务的达成,监控并且推动设备、人员和物料效率等经济指标不断提高。
Leads/drive the problem solving to secure the production by cooperating with QA, process, TD and SCD etc.Monitor and drive OE/people efficiency and material efficiency improvement.
7.实施并维护精益的工作流程；应用DaMaWay，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。
Apply and maintain and implement the LEAN work processes. Initiate, participate and facilitate the continuous improvement activities on safety, quality, cost, delivery, motivation and environment through DaMaWay.
8.组织对操作人员进行目标设定及定期跟进与考评。
PDR/IDP set up, communication and follow up.
9.支持公司安全、环境、健康及质量方面的审核，如WISE, ISO14001, GMP, ISO13485, Crisis and pre-package审核以及其他业务需求的审核。
Contribute and support company audits in safety, environment, health and quality sides, i.e. WISE, ISO14001, GMP, Specific GMP, ISO13485, Crisis and pre-package, and other audits which required by business needs.
10.上级主管或经理安排的其它工作
Other duties assigned by N+1 supervisor or manager.


任职要求：
1. 大专以上学历, 工科背景
College degree education or above, with majored in Engineering
2. 2年以上生产计划或生产管理的经验
2+ years working experience in production management or project management.
3. 卓越的自主意识和领导力，能开放的倾听和沟通，善于建立愿景和激发他人，能有效授权及实干
Excellent ownership and leadership, be good at commitment, open, empowerment and doer
4. 良好的沟通能力和团队合作精神
Easy communication, good team player.
5. 教导技能，能鼓励和被信服，善于不同人打交道，易沟通
Teaching skills, able to motivate and convince. Easy contact and interaction with different types of personalities.

其他要求

招聘人数：1人
职能类别：生产主管/工段长

公司介绍

具有百年历史的纽迪希亚公司是欧洲最大的专业肠内营养公司之一。进入中国市场十年以来，各项业务快速发展。于2000年投资2000万美金，成立了在中国的独资制药企业--纽迪希亚制药（无锡）有限公司，生产和销售响誉世界的肠内营养产品。今天，快速发展的纽迪希亚制药（无锡）有限公司，诚邀积极进取的您加盟，与纽迪希亚公司共同发展！

纽迪希亚制药（无锡）有限公司上海分公司主要负责公司产品在全国的销售。目前拥有员工超过800名。

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