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工作職責(zé)/Job Responsibility ? 制藥設(shè)備從海外工廠轉(zhuǎn)移以及本土化工作，并為本地制造和降低成本提供技術(shù)支持； Pharma machine transfer from COC and localization. And Technical support for local manufacturing and cost reduction; ? 根據(jù)客戶需求提供相應(yīng)的技術(shù)解決方案并執(zhí)行，包括零部件選型、零件清單、制圖以及支持安裝、調(diào)試等相關(guān)工作； Provide technical solution acc. to the requirements from customer and project fulfillment, including components type selection, BOM, drawing and technical support to assembly and installation; ? 負(fù)責(zé)產(chǎn)品專利的申請(qǐng)，了解競(jìng)爭(zhēng)對(duì)手對(duì)我們產(chǎn)品的侵權(quán)行為； Be responsible for patent application, get to know the patent infringement from the competitors; ? 支持分析市場(chǎng)和競(jìng)爭(zhēng)對(duì)手，了解市場(chǎng)和客戶需求； Make supports for market and competitor analysis, and get to know the requirements from the market and customers; ? 產(chǎn)品新功能的開(kāi)發(fā)、測(cè)試、更新以及版本管理； New product function development, testing, updating and version control; ? 監(jiān)控產(chǎn)品制造成本。優(yōu)化產(chǎn)品設(shè)計(jì)工作方法和流程，提高設(shè)計(jì)效率，優(yōu)化機(jī)加工零件的設(shè)計(jì)和制造工藝，降低物料成本； Product manufacturing cost monitoring, optimize product design method and process to improve design efficiency, and optimize machining components design and manufacturing process to reduce material cost; ? 產(chǎn)品知識(shí)體系的維護(hù)，包括建立和更新產(chǎn)品技術(shù)文檔體系，并組織經(jīng)驗(yàn)總結(jié)，負(fù)責(zé)產(chǎn)品機(jī)型工程師的培養(yǎng)和發(fā)展； Product know-how system maintenance, including product technical documentation system establishment and updating, and organize experience summary, and responsible for product engineer development; 工作要求/Job Requirement ? 8年以上相關(guān)行業(yè)工作經(jīng)驗(yàn)，制藥設(shè)備工作經(jīng)歷優(yōu)先； 8 years related industry working experience, solid pharmaceutical work experience is preferred; ? 本科以上學(xué)歷，制藥工程和機(jī)械等相關(guān)專業(yè)優(yōu)先； Bachelor or above degree is required, pharmaceutical engineering, mechanical or other related background are preferred; ? 英語(yǔ)口語(yǔ)流利，可以作為日常工作溝通語(yǔ)言； Fluent English speaking, and be used as daily work language; ? 熟悉《藥品生產(chǎn)質(zhì)量管理規(guī)范》和其它相關(guān)制藥行業(yè)法規(guī)； Deep knowledge of GMP and other related pharmaceutical rules and regulations; ? 熟悉Solidworks, Auto CAD, MS office, SAP等相關(guān)工作軟件； Good skill of Solidworks, Auto CAD, MS Office, SAP and other related working software; ? 具有獨(dú)立分析問(wèn)題的能力，能提出適當(dāng)?shù)慕鉀Q方案并進(jìn)行論證； Have the ability to analyze problems independently, can propose appropriate solutions and make demonstration; ? 自我驅(qū)動(dòng)力強(qiáng)，具有創(chuàng)新的思維方式。能獨(dú)立并有預(yù)見(jiàn)性的主動(dòng)開(kāi)展工作，能發(fā)現(xiàn)問(wèn)題并積極尋求解決方案； Self-driven, open, inspirational and innovation. Ability to work independently and predictably to identify problems and seek solutions actively; ? 具有項(xiàng)目管理經(jīng)驗(yàn)、組織協(xié)調(diào)能力、團(tuán)隊(duì)合作意識(shí)和良好的溝通能力； Project management skill, organization and coordination skills, teamwork awareness and good communication skills; ? 愿意承擔(dān)責(zé)任，并能贏得他人信任。在觀念和主動(dòng)性方面能以身作則，并影響他人； Be willing to take responsibility, and can get trust from others. Lead by example in the aspects of concept and imitative, and make influence to others; ? 良好的全局觀，能從公司角度考慮行為和方案所產(chǎn)生的結(jié)果和影響； A good global view, have the ability to consider the influence of the behavior and the solution from the perspective of the company；