主要職責：1. 負責公司產(chǎn)品的售后維修及維保工作, 偏工藝優(yōu)化方向2. 參與編制設(shè)備維修保養(yǎng)巡檢及預(yù)防性維護計劃；3. 對設(shè)備的故障原因進行分析匯總，落實改進方案實施.4. 結(jié)合當前數(shù)智化技術(shù)對客戶的維保提出建設(shè)性建議.5. 對客戶的售后服務(wù)請求做到快速響應(yīng),及時處理,提高客戶滿意度,保持良好的客戶關(guān)系；負責客戶的現(xiàn)場技術(shù)培訓；任職要求：1. 要求工作5~6年，本科以上學歷，生物工程或制藥工程相關(guān)專業(yè)2. 制藥工程專業(yè)者優(yōu)先，有藥企工程部工作經(jīng)驗者優(yōu)先；3. 要求有較強的服務(wù)意識和一定的市場銷售意識，較強的學習和問題分析總結(jié)能力；4. 要求有較強的溝通能力, 方案及項目計劃制定能力；5. 具有一定的吃苦精神，并愿意接受短期高頻次出差；6. 熟練掌握AutoCAD軟件。

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(shè)計、生產(chǎn)和銷售于一體。
為適應(yīng)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(shè)備工程有限公司，專業(yè)設(shè)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(shè)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(shè)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(shè)備、先進的檢測設(shè)備，主要生產(chǎn)設(shè)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(wù)、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.