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    更新于 12月24日

    工藝技術(shù)員

    5千-7千
    • 宿遷宿豫區(qū)
    • 1年以下
    • 大專
    • 全職
    • 招5人

    職位描述

    崗位職責(zé):
    1.督促員工嚴(yán)格執(zhí)行工藝規(guī)程各項(xiàng)參數(shù),起草實(shí)施在產(chǎn)產(chǎn)品的工藝驗(yàn)證;
    2.負(fù)責(zé)生產(chǎn)中出現(xiàn)的異常情況排查并解決,每日做好工藝巡察并有相關(guān)記錄;
    3.負(fù)責(zé)部門文件,記錄,資料的管理及崗位生產(chǎn)數(shù)據(jù)整理與匯總;
    4.負(fù)責(zé)產(chǎn)品生產(chǎn)前預(yù)算與單耗計(jì)算,產(chǎn)品生產(chǎn)結(jié)束后負(fù)責(zé)收得率計(jì)算,如收得率不在理論范圍內(nèi)并分析可能產(chǎn)生的原因;
    5.負(fù)責(zé)與質(zhì)量部門溝通生產(chǎn)情況,做好涉及到的偏差或變更與年度質(zhì)量回顧工作,起草實(shí)施清潔驗(yàn)證及設(shè)備確認(rèn);
    6.負(fù)責(zé)生產(chǎn)物料的登記管理,定期做生產(chǎn)質(zhì)量匯總并上報(bào);
    7.負(fù)責(zé)各崗位生產(chǎn)記錄與設(shè)備相關(guān)記錄的發(fā)放、收回與保管,收回的記錄審核后上交QA;
    8.參與編制部門培訓(xùn)計(jì)劃、組織培訓(xùn)及培訓(xùn)檔案的收集管理;
    9.生產(chǎn)過程中督促員工嚴(yán)格執(zhí)行GMP相應(yīng)條款;
    10.監(jiān)督崗位衛(wèi)生,與設(shè)備清潔狀況,做好生產(chǎn)車間與辦公區(qū)域環(huán)境衛(wèi)生與物品擺放,嚴(yán)格執(zhí)5S管理要求;
    11.配合研發(fā)中心做好與生產(chǎn)相關(guān)的小試、驗(yàn)證數(shù)據(jù)收集與整理工作;
    12.完成車間主任臨時(shí)安排的其它事項(xiàng);
    任職要求:
    1.分析化學(xué)、有機(jī)化學(xué)、藥物分析、藥物合成、制藥工程、藥品質(zhì)量安全管理等相關(guān)專業(yè)專科以上學(xué)歷;
    2.具有化學(xué)、藥學(xué)和GMP等相關(guān)法律法規(guī)知識;
    3..誠實(shí)守信,具有團(tuán)隊(duì)合作精神;良好的溝通能力和組織能力;
    上班時(shí)間:八小時(shí)工作制,雙休
    工作地點(diǎn):宿遷宿豫區(qū)生態(tài)化工科技產(chǎn)業(yè)園揚(yáng)子路20號,非常***!

    工作地點(diǎn)

    宿遷生態(tài)化工科技產(chǎn)業(yè)園揚(yáng)子路20號

    職位發(fā)布者

    許娜/人力資源經(jīng)理

    立即溝通
    公司Logo江蘇慈星藥業(yè)有限公司
    江蘇慈星藥業(yè)有限公司成立于2013年,座落于中國江蘇宿遷市生態(tài)科技產(chǎn)業(yè)園揚(yáng)子路20號,是專業(yè)生產(chǎn)銷售醫(yī)藥原料藥、藥用輔料、醫(yī)藥中間體的制藥公司,公司現(xiàn)有員工120人,擁有高級技術(shù)管理人員25人。公司擁有一套完整的合成加工和成品包裝車間,并建好6500平米符合新版GMP要求的凈化車間。公司成立以來,在客商的鼎立支持和全體員工的努力下,得到迅速發(fā)展,目前擁有準(zhǔn)字號原料批文18個(gè)。并具有規(guī)范的質(zhì)量管理體系及先進(jìn)的質(zhì)量控制手段。部分產(chǎn)品已通過PQ認(rèn)證。產(chǎn)品執(zhí)行 CHP、 USP、 EP、 BP等國內(nèi)、國際標(biāo)準(zhǔn)。Jiangsu Ci Xing Pharmaceutical co., LTD., founded in 2013, is a professional pharmaceutical company specialized in manufacturing and selling active pharmaceutical ingredients, pharmaceutical excipients and medical intermediates located in No.20, Yangzi Road, Ecological Science and Technology Industrial Park, Suqian City, Jiangsu, China with an existing staff of 120 people, including 25 senior technical managers. The company has an integrated workshop for synthetic processing and product packaging as well as a built purification plant of 6,500 square meters that meets the requirements of new GMP. Ever since its establishment, the company has been developing rapidly based on firm support of our merchant customers and endeavor of the whole staff. Currently the company has 18 medicine ingredients’ approved numbers, standard quality management system and advanced quality control means. Part of our products have been certified by PQ. All our products are in accordance with domestic or international standards including CHP, USP, EP, BP and so on.江蘇慈星藥業(yè)有限公司擁有一批致力于醫(yī)藥事業(yè)的各類年輕的專業(yè)技術(shù)及管理人才的同時(shí),仍向社會(huì)廣招賢才,力爭把新品研發(fā)與技術(shù)改造、質(zhì)量管理與質(zhì)量控制、產(chǎn)品銷售與服務(wù)、生產(chǎn)與設(shè)備管理等方面精于求精,更上一層,勇于創(chuàng)新,積極進(jìn)取,在不久的未來江蘇慈星藥業(yè)有限公司將會(huì)在醫(yī)藥原料藥合成領(lǐng)域做得更好,走的更遠(yuǎn)。Despite equipped with a group of all kinds of young professional technical and management talents who dedicate themselves to medicine business, Jiangsu Ci Xing Pharmaceutical co., LTD. still seeks more talents from the society. We are striving to be better, advanced, more creative and more aggressive in all aspects including new product development, technical innovation, quality management, quality control, product sales, customer service, production and equipment management. In the near future, Jiangsu Ci Xing Pharmaceutical co., LTD will do a better and further job in the field of active pharmaceutical ingredients synthesis.
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