# Quality Associate Director, MCOQ at AstraZeneca

AstraZeneca is hiring a Quality Associate Director, MCOQ. Level rates it Little AI ●○○○; you can [apply on Level](https://jobsbylevel.com/go/28f98ab6-7ec3-4b6a-b34a-a978f53b410a?utm_medium=ai-agent).

AI Level 1, AI centrality 29 out of 100. Qingdao Office.

## Details

- Company: [AstraZeneca](https://jobsbylevel.com/companies/astrazeneca)
- AI level: AI Level 1 (score 29 out of 100)
- Location: Qingdao Office
- Posted: October 12, 2026
- Apply: https://jobsbylevel.com/go/28f98ab6-7ec3-4b6a-b34a-a978f53b410a?utm_medium=ai-agent

## Description

Core Accountabilities: Develop, support and drive excellence in MCOQ GMP&GDP Quality activities to maintain the local License to Operate. Participates in defining the strategy for the commercial global markets ownership and execution of MCOQ GMP and GDP Quality System and framework in country Define, develop, deploy and monitor the GMP/GDP policies and standards and execution in country markets Supports local MC to deliver the license to operate, including but not limited to support for GMP&GDP/GSP audits and inspections, implementation effective self-inspection programs in the country of responsibility. Responsible for ensuring QMS compliance and continuous improvement in the Region and all issues are managed and closed on time, risks are identified and escalated to Global Quality. Represents Quality on cross-functional and cross SET teams and steering committees related to MC market Drive global standardisation, simplification, and improvement of MCOQ Quality business processes. Develops and sustains a high-quality organisation that delivers against global processes, and aims to continuously improve in competence, compliance standards and innovative delivery of results. Provide training, supporting and coaching structure for Quality MCOQ network roles Participates in strategy and objectives setting for the MCOQ organisation Accountable for compliance assurance and working to one set of GMP & GDP/GSP standards and processes, as well as common GxP process across the MC GxPs. Accountable for both GSP regulatory and AZ standards related to distribution of AZ product in country, including but not limited to release of product batched, resolution of Issue Management, recalls, influence and decisions on local regulatory agency interactions, audits and inspection readiness and compliance to gain and maintain AZ licence to operate. To be part of global vendor program management, support AZ finished products management and work with sending site QA, EQ and global cooperate quality. Demonstrated ability to work independently and in project settings to deliver objectives. Keeps own knowledge of best practices, industry standards and new developments in quality management up to date Leads trouble shooting activities to resolve existing problems, make complicated judgements and anticipate future developments in AstraZeneca’s Quality related needs Employs prepared information to discuss, plan and help carry out improvement plans, priority setting, investigation reports, quality or performance improvement recommendations Carries out compliance reviews and reporting for external suppliers including issue resolution with senior management Contribute to Quality function in developing quality management system to fulfil Good Supply Practice (GSP) and AstraZeneca standards to ensure continuous improvement. Responsible for the assessment and implementation of regulatory and AZ policy & standards requirements. For process and procedure impacted multiple areas, represent China MCOQ Quality to correspond with other function. Promotes a Quality Culture in the MC sets strategy in the region and locally for execution of GMP/GDP excellence. Responsible for the achievement of country KPIs and objectives/Quality Plans. Ensure country trends are addressed through development of country continuous improvement plans. Contributes to development procedures in area of specialism and provides some technical input into the development of global standards for function and globally Proactively looks for opportunities to identify change and make efficiency savings, influence decisions and deliver the results whilst ensuring and appropriate level of compliance 在MCOQ的GMP与GDP质量活动中进行开发、支持并推动卓越表现，以维持本地药品批发企业的经营许可（License to Operate）。 参与制定商业全球市场在本国范围内对MCOQ的GMP与GDP质量体系及框架的所有权与执行策略。 定义、制定、部署并监控GMP/GDP流程、标准及其执行情况。 支持本地市场公司（MC）维持GSP证照维护，包括但不限于支持GMP/GDP/GSP审计与检查，以及在负责国家实施高效的自检计划。 负责确保区域层面的QMS合规与持续改进，确保所有问题按时管理与关闭，风险得到识别并上报至全球质量团队。 在与市场公司市场相关的跨职能、跨SET团队及指导委员会中代表质量职能。

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Source: https://jobsbylevel.com/jobs/quality-associate-director-mcoq-at-astrazeneca-f956f2

## Cite this page

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