• 8-9年经验
  • 本科
  • 招若干人
  • 11-09 发布

职位描述

职位描述: 领导QA部门一起维护和提高产品的质量,维护公司的声誉,和强生公司的品牌。将质量体系贯彻到公司的各个领域, 包括原材料, 采购, 生产, 检测,贮存和货运。Lead plant QA team to maintain product quality and continuous improvement. Ensure implementation of the quality system in whole product lifecycle, including raw material, purchasing, production, testing, storage and distribution, etc.?严格监控和质量相关的各个活动,包括采购、生产、检测、贮存、货运等各个环节,并协助各部门做好生产现场管理工作,使得产品生产的全过程都在严密的监控下进行。Manage GMP which covers all matters, which individually or collectively influence the quality of product.?负责生产/质量管理有关程序的起草、审核和批准。Responsible for initial, review and approval of applied procedure of production/quality.?负责批生产记录和批检验记录的审核,经授权后释放产品。Responsible for review of batch record and testing report; responsible for finished product release when authorized.?参与各类验证文件的审阅及验证活动的监督。Review validation documents and conduct supervision when necessary.?负责变更控制和变更的审核。Responsible for Change control review.?负责偏差的管理和调查,在适当的时候签发预防纠正措施,并负责进行追踪和评估。Responsible for non-conformance investigation and management, approve, tracking and evaluate CAPA when necessary.?负责质量相关客户投诉的调查及监督纠正与预防措施的执行。Responsible for quality related customer complaint investigation and implantation of CAPA when necessary.?负责管理并协调本部门员工项目安排,制定并实施培训计划。Responsible people development including training of responsible department.?负责产品的年度质量回顾。Responsible for product annual review.?负责不合格品的批准和监督处理的执行(如返工、销毁)。Responsible for reject material and finished products approval, as well as the destruction process.?负责返回产品的处置批准。Responsible for returned products disposition approval.?参与内部和外部的审计。Participate in internal and external audits.?遵守环境、安全和健康准则。Comply with EHS requirements.?遵守公司的规章制度和HCC的规定。Comply with company rules and regulations and HCC policy?有义务按公司投诉程序将客户投诉电话转至相关部门。Be obliged to transfer the customer complaints to relevant department under customer compliant procedure; and involve in the handling of customer complaints if necessary;?上级主管交付的其它相关工作Other work assigned by supervisorQualifications:五年以上工作经验,熟悉GMP体系,具有在制药行业的质量管理经验,了解如何制定质量标准和标准操作程序,有组织和管理能力,对原材料和生产过程控制比较熟悉。-5 years above working experience in related industry including the quality management experience in pharmaceutical industry.-Familiar with GMP system-Strong leadership-Familiar with SOP initiation, review and approval process-Familiar with raw materials and manufacturing control process. 职能类别: 质量管理/测试经理(QA/QC经理) 药品生产/质量管理

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公司信息

拥有125年历史的美国强生公司是世界上最具综合性、业务分布范围最广泛的健康护理产品的制造和服务企业,为消费品、制药以及医疗器材和诊断产品市场提供全面的产品和服务。强生公司连续多年名列《财富》“全球最受尊敬的公司”排行榜前列。 强生公司一致注重在中国的发展,强生(中国)有限公司1992年在上海市闵行经济技术开发区成立,是强生公司在中国大陆设立的首家独资企业,致力于生产和推广高品质的适合各种年龄段的个人卫生护理用品,推动中国家庭健康护理水平的提高,公司的产品不仅供应国内消费品市场,而且还出口供应国际市场。强生(中国)有限公司的使命是成为中国最受信赖的消费类健康保健公司。公司致力于生产和销售高品质的个人保健产品,以增进中国家庭的健康。 With more than 100 years of history, Johnson & Johnson (JNJ) is the world’s most broadly based healthcare company discovering, developing, and manufacturing consumer health, pharmaceuticals, and medical devices and diagnostics products. With over 250 operating companies, Johnson & Johnson has approximately 114,000 employees in 57 countries and markets its products throughout the world. It has been ranked among the top of the global Most Admired Companies by Fortune for years. Johnson & Johnson has been committed to its development in China. Established in Shanghai Minhang Economic & Technological Development Zone in January 1992, Johnson & Johnson China Ltd. is the first wholly-funded enterprise set up by Johnson & Johnson. It is committed to producing and promoting high quality personal health care products catering for consumers of various ages, and driving the health care of Chinese families. Its products are not only sold in domestic consumer market, but also exported to international markets. The mission of Johnson & Johnson China Ltd. is to become the most reliable consumer health care product provider in China. It is committed to producing and selling high quality health care products to enhance the health of Chinese families. 更多机会请登陆www.careers.jnj.com 强生消费品中国今年启动了校招微博,我们将在第一时间公布校招信息和校招进程,请@强生消费品中国-校园招聘。

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