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Associate Director Quality Control
2-4万
人 · 本科 · 10年及以上工作经验 · 性别不限2025/05/05发布

城阳区汇智桥路151号中科研发城A2

公司信息
阿斯利康制药有限公司

外资(欧美)/500-1000人

该公司所有职位
职位描述
Location: Qingdao Site
This is a role as the principal quality control engineer in the leading edge project of new pMDI manufacturing facility in China.
The role incumbent will
Provide 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 required
The 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 Responsibilities
Provide 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.

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