Quality Digital Principal Engineer
職位描述
* Support digital use cases as Quality SME combined quality professional and digital capability to ensure compliance to PQS, cGMP and regulation interfacing between QA/compliance and digital operation. * Support development of GPQS, ECMS, GVLMS,SAP database and provide oversight and expertise. * Leading/implement site quality digital transformation plan, uplifting organization digital capability. * Introduce/implement/support digital use case to achieve the quality improvement. * Support the daily affairs of quality-related systems. Promote the integration and optimization of systems and related business processes. * Improve the visualization of quality business, develop data analysis capabilities. Provide support for different quality tiers to make decisions based on data. * Build the innovation culture and improve the digital ability of Quality Assurance Function. * Manage QAF’s digital applications to support daily business. * Participate in the develop of quality management strategy for new technology. Ensure the projects delivering and related validation activities meet the requirements of GMP regulations and quality requirements. * Conduct activities and interactions consistent with Company Values and in compliance with the Code of Ethics and supporting Policies and Standards relevant to your role (including SHE).? Complete all required training on the AZ Code of Ethics and supporting Policies and Standards on time.??Report potential issues of non-complianceEducation, Qualifications, Skills and ExperienceEssential * Bachelor’s degree and general experience in pharmaceutical quality, manufacturing, or technical roles. * A good knowledge of cGMPs and global GMP requirements, quality systems, and pharmaceutical product/device testing technology and pharmacopeia. Well -developed interpersonal and problem-solving skills. * Have computerized system related working experience? * A basic knowledge of computer validation requirements and 21 CFR 11 requirements. * Demonstrated ability to work independently and collaboratively on multidisciplinary and multifunctional. * Use both Chinese and English as working language. * Excellent oral and written communication skills with the ability to communicate effectively with individuals from all levels of the organization.Desirable * Experience within a complex dynamic business environment * Device manufacturing/quality supervisory/management experience * Lean / six sigma manufacturing training and applied experience * In-depth experience with project management * Embracing change and innovation and actively seek ways to simplify and standardize across the Quality network
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