職位描述
職位概要:1.針對客戶物料,進行相關(guān)的試驗,進行選材;2.審核施工圖,對施工圖提出審核意見;3.根據(jù)設備或工程結(jié)構(gòu)特點,進行焊接工藝評定、焊工培訓、編制相應的焊接工藝文件(主要闡述施工的方法、要點及相關(guān)注意事項以及檢驗方法)和進行焊接技術(shù)創(chuàng)新等;4.根據(jù)公司發(fā)展,提出需要的工藝裝備或焊接設備;5.依據(jù)具體的項目要求,提出焊接材料需求計劃;6.處理施工過程中出現(xiàn)的焊接技術(shù)問題7.進行工藝紀律檢查,糾正不當行為8.協(xié)助相關(guān)部門進行分包商審核及技術(shù)管理工作;9.經(jīng)驗總結(jié)任職要求:1.焊接類化學類或材料類相關(guān)專業(yè)本科及以上學歷。2.受過機械類或工程類焊接等方面的培訓。3.一年以上焊接工藝編制工作經(jīng)驗,熟悉焊接工藝;4.具有較強的語言表達能力、人際交往能力、應變能力、溝通能力及解決問題的能力;5.熟悉現(xiàn)行壓力容器、管道和鋼結(jié)構(gòu)的焊接標準及規(guī)范;6. 英語水平良好;
企業(yè)介紹
森松集團(中國)系日本森松工業(yè)株式會社(創(chuàng)立于1947年)的全資集團。1990年,公司作為首家外資企業(yè)進駐上海浦東新區(qū),集開發(fā)、設計、生產(chǎn)和銷售于一體。
為適應更加專業(yè)化生產(chǎn)的需要,森松集團(中國)于2001年成立了上海森松制藥設備工程有限公司,專業(yè)設計、生產(chǎn)和承接制藥、生物工程、化妝品、食品、電子、精細化工等行業(yè)和領(lǐng)域各種成套設備、衛(wèi)生級容器和換熱器、潔凈公用工程系統(tǒng)、無菌工藝管道、CIP在線清洗工作站、生物發(fā)酵和細胞培養(yǎng)系統(tǒng)和生物工程上下游模塊,以及均質(zhì)系統(tǒng)、WD三合一等。公司能根據(jù)客戶要求,分別符合SFDA、FDA、EMEA或WHO等相關(guān)的GMP要求進行設計和制作,并提供相關(guān)的驗證支持文件。公司擁有先進的生產(chǎn)技術(shù)、齊全的生產(chǎn)設備、先進的檢測設備,主要生產(chǎn)設備及測試儀器從德、美、日等國家進口;同時,公司擁有技術(shù)精湛的專業(yè)人員、優(yōu)量的售后服務、嚴格的質(zhì)量保證體系,公司的所有流程均有嚴格的質(zhì)量體系,并通過了ISO9001質(zhì)量體系認證。
Morimatsu Industry Ltd. (Japan) was founded in 1947. Morimatsu (China) Group, fully invested by Morimatsu Industry Ltd., is the first foreign invested company founded in Shanghai Pudong new area in 1990, and engaged in development, design, fabrication and marketing.
To meet the requirement of much more professional and specialized production, Morimatsu (China) Group founded Shanghai Morimatsu Pharmaceutical Equipment Engineering Co., Ltd. in 2001. The company is professional in designing and fabricating complete equipment, sanitary vessels and heat-exchangers, sanitary facilities piping system, sterile process piping system, CIP workstation, fermentation and cell cultivation system, bioengineering upstream to downstream skids, homogenizing system, WD multi-functional filter etc. These products and system have been widely used in pharmaceutical, bio-engineering, cosmetic, food process, electronic, and fine chemical industries. Based on clients’ requirement, the company can meet relevant GMP of SFDA, FDA, EMEA or WHO, and provide relevant validation support documents. The company possesses advanced technology, complete production facilities, advanced testing devices, and the main production facilities and testing devices are imported from Germany, America and Japan. On the same time, the company also has excellent technical personnel, satisfactory after-sale service and strict quality assurance system. All production processes are controlled under the quality assurance system, and the company has passed ISO9001 quality system certification as well.