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(yè)簡(jiǎn)介
阿斯利康是全球領(lǐng)先制藥公司,由前瑞典阿斯特拉公司和前英國(guó)捷利康公司于1999年合并而成。阿斯利康在6大治療領(lǐng)域?yàn)榛颊咛峁└挥趧?chuàng)新,卓有成效的醫(yī)藥產(chǎn)品,包括消化、心血管、腫瘤、中樞神經(jīng)、麻醉和呼吸等,其中許多產(chǎn)品居于世界領(lǐng)先地位。
阿斯利康總部位于英國(guó)倫敦,研發(fā)總部位于瑞典。產(chǎn)品銷(xiāo)售覆蓋全球100多個(gè)國(guó)家和地區(qū)。2005年公司銷(xiāo)售收入為240億美元。
阿斯利康擁有強(qiáng)大的研發(fā)能力,平均每個(gè)工作日的研發(fā)投入達(dá)到1400萬(wàn)美元 (2005年研發(fā)總投入為34億美元)。我們?cè)?個(gè)國(guó)家設(shè)有11個(gè)研發(fā)機(jī)構(gòu),共有11,900名員工從事與新藥研發(fā)相關(guān)的工作。
阿斯利康擁有極具希望的早期開(kāi)發(fā)產(chǎn)品組合,共有45個(gè)項(xiàng)目處于臨床前研究階段、17個(gè)項(xiàng)目處于一期臨床研究階段、13個(gè)項(xiàng)目處于二期臨床研究階段、6個(gè)項(xiàng)目處于三期臨床研究階段。
阿斯利康在全球19個(gè)國(guó)家有27個(gè)生產(chǎn)基地,共有14,000名員工致力于為客戶(hù)提供安全、有效、高質(zhì)量的產(chǎn)品。
阿斯利康在全球共有65,000名員工,從事醫(yī)藥產(chǎn)品和醫(yī)療服務(wù)的研發(fā)、生產(chǎn)和銷(xiāo)售業(yè)務(wù)。
阿斯利康被列入道瓊斯可持續(xù)發(fā)展指數(shù)(全球)以及顯示企業(yè)良好社會(huì)責(zé)任度的富時(shí)社會(huì)責(zé)任指數(shù)(FTSE4Good Index)。
職位發(fā)布企業(yè)

阿斯利康制藥公司
企業(yè)性質(zhì):
企業(yè)規(guī)模:1-49人
成立年份:
企業(yè)網(wǎng)址:http://www.chnequestrian.com
企業(yè)地址:海淀區(qū)
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職位發(fā)布日期: 2025-03-31