Associate Director Quality Control
職位描述
Location:?Qingdao SiteThis is a role as the principal quality control engineer in the leading edge project of new pMDI manufacturing facility in China.The role incumbent willProvide 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.?Design and lead the automation digital processes to support QC business.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 requiredThe 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 make decisions for quality control issues and actively communicates with colleagues.??Job ResponsibilitiesProvide 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.
企業簡介
阿斯利康是全球領先制藥公司,由前瑞典阿斯特拉公司和前英國捷利康公司于1999年合并而成。阿斯利康在6大治療領域為患者提供富于創新,卓有成效的醫藥產品,包括消化、心血管、腫瘤、中樞神經、麻醉和呼吸等,其中許多產品居于世界領先地位。
阿斯利康總部位于英國倫敦,研發總部位于瑞典。產品銷售覆蓋全球100多個國家和地區。2005年公司銷售收入為240億美元。
阿斯利康擁有強大的研發能力,平均每個工作日的研發投入達到1400萬美元 (2005年研發總投入為34億美元)。我們在7個國家設有11個研發機構,共有11,900名員工從事與新藥研發相關的工作。
阿斯利康擁有極具希望的早期開發產品組合,共有45個項目處于臨床前研究階段、17個項目處于一期臨床研究階段、13個項目處于二期臨床研究階段、6個項目處于三期臨床研究階段。
阿斯利康在全球19個國家有27個生產基地,共有14,000名員工致力于為客戶提供安全、有效、高質量的產品。
阿斯利康在全球共有65,000名員工,從事醫藥產品和醫療服務的研發、生產和銷售業務。
阿斯利康被列入道瓊斯可持續發展指數(全球)以及顯示企業良好社會責任度的富時社會責任指數(FTSE4Good Index)。
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職位發布日期: 2025-03-31