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sophia85919新蟲(chóng) (初入文壇)
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[交流]
人福醫(yī)藥集團(tuán)---人福普克藥業(yè)（武漢）有限公司誠(chéng)聘QA Specialist
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人福醫(yī)藥集團(tuán)---人福普克藥業(yè)（武漢）有限公司誠(chéng)聘QA Specialist 人福普克藥業(yè)（武漢）有限公司是人福醫(yī)藥集團(tuán)在武漢生物醫(yī)藥產(chǎn)業(yè)園投資建立的高質(zhì)量的國(guó)際制藥企業(yè)，產(chǎn)品涵蓋多種劑型的美國(guó)處方藥/非處方藥，面向歐美主流市場(chǎng)。 本公司具有世界級(jí)的管理團(tuán)隊(duì)和技術(shù)力量，有良好的企業(yè)文化和發(fā)展前景，提供專(zhuān)業(yè)培訓(xùn)和有競(jìng)爭(zhēng)力的待遇，誠(chéng)邀精英加盟，共同打造世界級(jí)制藥企業(yè)。 Located in Wuhan Bio-Pharmaceutical Industrial Park, PuraCap Pharmaceutical Corporation is a brand new state-of-the-art manufacturing plant invested by U.S. Puracap Pharmaceutical LLC, which is head-countered in New Jersey, USA. We are excellent in the U.S. FDA CGMP manufacturing standards. With world-class management team and technical strength, PuraCap Pharmaceutical has an excellent corporate culture and development prospects. We invite you to join us and work together to build a world-class pharmaceutical company. Essential Responsibilities： 1、To be responsible for batch disposition and has the authority to determine whether finished products are released for marketing or not. 2、To be oversight for monitoring process during all the manufacturing and packaging process, assurance all process and operations in compliance with cGMP regulations and site quality requirements. 3、To review or approve the validation report and quality monitoring during validation process. 4、To be responsible for the annual product review 5、To deal with deviations, changes, complaints related to responsible products 6、Other QA jobs including procedure review assigned by supervisor Qualifications任職要求： 1、Bachelor degree or above, majored in pharmaceuticals,chemistry or related sciences. 化學(xué)制藥相關(guān)專(zhuān)業(yè)專(zhuān)科以上學(xué)歷 2、 over three years of experience in production or QA. 有3年以上制藥企業(yè)生產(chǎn)及質(zhì)量工作背景； 3、Excellent English in reading and writing;良好的英語(yǔ)讀寫(xiě)能力 4. Responsible, excellent communication and coordination skills, strong learning ability.有較強(qiáng)的責(zé)任感及良好的溝通能力 5．Familiar with cGMP and FDA regulation preferred. 參加過(guò)FDA或GMP認(rèn)證者尤佳，具備內(nèi)審員資格或供應(yīng)商管理方面的經(jīng)驗(yàn)者更佳。 簡(jiǎn)歷投遞郵箱：zhaopin@renfu.com.cn [ Last edited by sophia85919 on 2012-4-23 at 15:22 ] |
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