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AstraZeneca is seeking an Associate Director of Quality Control in Qingdao, China, to ensure compliance with GMP requirements during the development of a new pMDI manufacturing facility. The role involves overseeing various quality functions, mentoring staff, and ensuring operational effectiveness throughout the project's lifecycle.
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Job Summary
Provide Quality support to achieve the pMDI project milestones and ensure compliance with GMP requirements during the entire life-cycle of the Qingdao capital project initiative.
Responsible for ensuring GMP compliance and operational effectiveness of the validation program, including facility, equipment, utility qualifications, computer system validation, cleaning validation, or process validation.
Interface with engineering, IT, QA, manufacturing, and technical functions on capital projects, proactively ensuring GMP compliance during design, construction, and start-up phases.
Matching Summary
Match Score: 75
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AstraZeneca is seeking an Associate Director of Quality Control in Qingdao, China, to ensure compliance with GMP requirements during the development of a new pMDI manufacturing facility. The role involves overseeing various quality functions, mentoring staff, and ensuring operational effectiveness throughout the project's lifecycle.
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Skills & Requirements
Must-have
GMP compliance
validation program oversight
Quality Systems expertise
China legislation knowledge
cGMP knowledge
lab systems and testing technology
Nice-to-have
cross functional interaction
automation digital processes
influencing stakeholders
diversity and equality
Key Requirements
Expert level understanding of China legislation
Expert level understanding of cGMPs
Expert level understanding of Validation
Expert level understanding of Quality Systems
Expert level understanding of deviations and change controls