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人福医药集团---人福普克药业（武汉）有限公司诚聘QA Specialist
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人福医药集团---人福普克药业（武汉）有限公司诚聘QA Specialist 人福普克药业（武汉）有限公司是人福医药集团在武汉生物医药产业园投资建立的高质量的国际制药企业，产品涵盖多种剂型的美国处方药/非处方药，面向欧美主流市场。 本公司具有世界级的管理团队和技术力量，有良好的企业文化和发展前景，提供专业培训和有竞争力的待遇，诚邀精英加盟，共同打造世界级制药企业。 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任职要求： 1、Bachelor degree or above, majored in pharmaceuticals,chemistry or related sciences. 化学制药相关专业专科以上学历 2、 over three years of experience in production or QA. 有3年以上制药企业生产及质量工作背景； 3、Excellent English in reading and writing;良好的英语读写能力 4. Responsible, excellent communication and coordination skills, strong learning ability.有较强的责任感及良好的沟通能力 5．Familiar with cGMP and FDA regulation preferred. 参加过FDA或GMP认证者尤佳，具备内审员资格或供应商管理方面的经验者更佳。 简历投递邮箱：zhaopin@renfu.com.cn [ Last edited by sophia85919 on 2012-4-23 at 15:22 ] |
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sophia85919
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