泰州招聘

Activities in the scope of the Manufacturing Process Engineer position include but are not limited to:

制造与工艺工程师职位责任范围包括但不限于：

? Coordinating, Performing, test, and Writing validations protocol and report of product, processes and equipment in accordance with FDA and ISO guidelines,

?按照FDA和ISO医疗器械制造标准下从事协调，执行,测试和写作工艺和设备验证议定书和报告书,
? Designing, executing, and analyzing experiments based on statistical techniques;developing, troubleshooting and refining medical device manufacturing processes and equipment consistent with engineering principles and lean principles,

?设计，执行和分析实验统计技术的基础上来开发,疑难排解,和改善医疗器械制造工艺和设备，符合工程原则和精益原则，

? Evaluating proposed improvements to processes and products based on analyses of regulatory requirements, product quality needs, safety, environmental, economics, and operational goals, etc.

?评估有关建议改进工艺和产品需基于分析相关监管要求，产品质量的需求,安全，环保, 经济，经营目标等

? Driving the efficient scale-up of manufacturing processes,

? 部门内主要驱动高效规模化的制造过程的人员，

? Writing procedures, training other associates, and assisting other technical associates.

?写程序，培训人员，并协助其它技术同仁

Requirements / Qualifications

要求/资格

? A degree in Science or Engineering is required. A minimum of 3 years of experience in an engineering capacity in the medical device, pharmaceutical, or food industry is required.

?科学或工程学位(大专视为同等)是必需的。至少需要3年相关经验，在医疗设备,医药, 戓食品行业内。

? Excellent written, oral and presentation skills are required.

?出色的书面，口头和表达技巧是必需的。

? A work style of hands-on involvement with all phases of his/her projects

实际参与工作作风

? Demonstrated ability to prioritize, initiate, and drive projects to completion,

?需在优先次序，启动和驱动项目/计划完成上展示工作能力

? knowledge of the fundamentals of statistics (SPC, Minitab…..)

?需有基本统计知识（如SPC，Minitab.....）

? Ability to work effectively in team situations as well as independently,

?有能力在团队情况下或独立运作下都能有效地开展工，

? demonstrated excellent communication skills, both written and oral (in Chinese/ mandarin). Able to read English (It is a big plus, if the candidate can read and write English)

?在书面和口语(普通话）展现出色的沟通能力。需能阅读英文.（如果应征者能阅读英文及写英语- 优先考虑）

? Working knowledge of GMP and ISO 9000 requirements.

了解GMP和ISO9000的要求。

赛昂国际医疗技术(中国)有限公司Scion Medical Technologies (China) Ltd.是由SCION MEDICAL LIMITED（赛昂国际医疗控股有限公司）于2011年10月在中国大陆投资创办的外商独资企业，中国运营总部和工厂位于中国医药城。赛昂中国一期投资壹亿人民币，生产面积7000平米，计划建设4条生产线和1个研发中心。
公司利用其在国际医疗器械领域丰富的管理和并购经验和人脉，收购并整合欧美的高端医疗技术并引进中国医药城园区，在园区打造国际化的医疗器械生产基地（园区）。降低生产成本，供应全球市场，在保持欧美销售增长同时，迅速在中国注册和销售并购的高端医疗器材。