Specialist Quality Control (Analytical Lab)

Typical Accountabilities 主要职责 Specific Responsibilities/Tasks Routine work 日常工作   • Finish the routine analytical work accurately and timely • undefined • Issue the analytical method transferring and validation protocol for raw materials finish products etc., • undefined • Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status. • undefined • Double-checking the BAR. • undefined • Responsible for the management of  chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory • undefined • Responsible for the handling and disposal of lab wasted articles/expire reagent/toxic substances • undefined • Keep the chemical lab tidy and clean at any time. • undefined • Report any deviation timely, lead major deviation/OOS investigation   • undefined • Stability study management • undefined • Issue and revise specification, test method and batch analysis record of starting materials and finished products, and purchasing specification, test method for PQ, CQ etc. • undefined • Prepare specification for application (draft) and specification explanation • undefined • Maintenance of QC E-system eg. GQCLIMS,1Lab, Empower •  /Empower • New employee training • undefined • Issue technical assessment report • undefined • Lead team level CI project • undefined S.H.E. Responsibilities SHE 职责 • Take personal responsibility for security to protect themselves and avoid harm to others and the environment • undefined • Participate the necessary security training and drills with the contingency project • undefined • Strictly enforce the job safety procedures • undefined • Report any incidents , accidents and hazards in work timely • undefined • Purchase/ store/ use controlled chemicals. • undefined GMP compliance GMP 符合性 • Strictly following SOP and Guideline   严格执行岗位操作规程和指南 • Take GMP training and strictly following GMP compliance               参加GMP培训，严格遵守GMP与法规要求 • Fill in related documentation such as BAR, other logbook etc., timely to ensure the accuracy of content as per requirement of SOPs. • undefined • Take part in actively in correction to the observations found in self-inspection.      积极参加对自检中所发现缺陷的整改 Training and development 培训和发展 • Participate actively in serials training required to be held by internal and external. • undefined • Develop all kinds of skills in relation to work field and pursue continuous improvement     发展各种工作技能并追求持续的改进 Others 其他 • Assist the senior engineer in completing tasks when required. • undefined • Complete other tasks arranged according to business needs      根据业务需要完成安排的其他工作 Qualifications资质 Education, Experience and Training 教育、工作经验和培训 Education, Experience and Training 教育、工作经验和培训 • Academic / Professional qualification 学历/专业资格 Bachelor or above 本科或以上学历 • Technical / skills training 技术/技能训练 Basic GMP, GLP knowledge; Experience in QC 基本的GMP, GLP知识及QC经验 • Working experience 工作经验 (No. of years / 年 资, Job function /工作功能, Business types /业务种类 ) - Essential 必需 More than 4 years working experience in pharmaceutical company or related industry 4年以上制药企业或相关行业的工作经验 - Desirable 理想 More than 5 years working experience in pharmaceutical company or related industry 5年以上制药企业或相关行业的工作经验 Capabilities 能力 • Language ability/ 语言能力 Fluent English skill in both oral and written 流利的英文交流和读写能力 • Computer literacy/电脑知识 Good computer skill 良好的计算机能力 • Communication ability/ 沟通能力 Good communication and presentation skills 良好的沟通和展示技能 • Others/ 其他 Good team work spirit 良好的团队合作精神 Sense of responsibility and work actively 富有责任心及工作积极 Date Posted 03-Nov-2026 Closing Date 30-Jan-2027 AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and dive