Senior Quality Control Engineer/Specialist
职位描述
Location: first 6-12 months in Jiangsu, permanent location in QingdaoThis is a role as the quality control specialist in the leading edge project of new pMDI manufacturing facility in China.The role incumbent will * Provide Quality support to achieve the pMDI project milestones. * Responsible for ensuring compliance with GMP requirements during the design, construction, start-up, validation (entire life-cycle) of Qingdao capital project initiative. * Ensuring GMP compliance and operational effectiveness of the validation program (facility, equipment, utility qualifications; computer system validation, cleaning validation or process validation). * Cross functional interaction with both internal and external colleagues in Operations and Quality to ensure full compliance with AZ standards and local regulations. * Mentor, train, and develop QC and other engineering / operations staff and interns in relevant technical subjects and is a key contributor to GMP training activities. * Supervise and oversight contractors and intern activities as required * Provide Quality expertise to the project and later site. * Influence site management and propose solution options to improve and/or resolve technical challenges. * Support development of GPQS, ECMS, GVLMS database and provide oversight and expertise. * Provide oversight / ownership of QMS including validation, change controls, deviations, and related infrastructure activities within the Qingdao Operations site. * Interface with engineering, IT, QA, manufacturing and technical functions on capital projects and proactively ensure GMP compliance during the design, construction and start up phases of the project. * Develop and drive necessary departmental process, documentation and training. * Develops and maintains technical competency and collaborates with counterparts in engineering, IT, QA, manufacturing and technical functions to provide Quality oversight in designated projects and activities. * Supports quality control efforts for GMP related facility and equipment systems to ensure full GMP compliance.The incumbent has expert level understanding of china legislation, cGMPs, Validation and Quality Systems, specifically deviations and change controls and maintains current knowledge of lab systems and testing technology.The incumbent is capable of influencing stakeholders and partners and be able to effectively problem solve complex quality control issues and actively communicates with colleagues.
企业简介
阿斯利康是全球领先制药公司,由前瑞典阿斯特拉公司和前英国捷利康公司于1999年合并而成。阿斯利康在6大治疗领域为患者提供富于创新,卓有成效的医药产品,包括消化、心血管、肿瘤、中枢神经、麻醉和呼吸等,其中许多产品居于世界领先地位。
阿斯利康总部位于英国伦敦,研发总部位于瑞典。产品销售覆盖全球100多个国家和地区。2005年公司销售收入为240亿美元。
阿斯利康拥有强大的研发能力,平均每个工作日的研发投入达到1400万美元 (2005年研发总投入为34亿美元)。我们在7个国家设有11个研发机构,共有11,900名员工从事与新药研发相关的工作。
阿斯利康拥有极具希望的早期开发产品组合,共有45个项目处于临床前研究阶段、17个项目处于一期临床研究阶段、13个项目处于二期临床研究阶段、6个项目处于三期临床研究阶段。
阿斯利康在全球19个国家有27个生产基地,共有14,000名员工致力于为客户提供安全、有效、高质量的产品。
阿斯利康在全球共有65,000名员工,从事医药产品和医疗服务的研发、生产和销售业务。
阿斯利康被列入道琼斯可持续发展指数(全球)以及显示企业良好社会责任度的富时社会责任指数(FTSE4Good Index)。
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职位发布日期: 2025-03-31