{"id":3677573,"url":"https://alion.io/job/astrazeneca-specialist-quality-control-analytical-lab-2","title":"Specialist Quality Control (Analytical Lab)","company":{"id":13195,"name":"AstraZeneca","domain":"astrazeneca.com","url":"https://alion.io/company/astra-zeneca","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":94,"open_postings":172,"ghost_share":0.012,"stale_share":0.366,"repost_share":0.105,"time_to_fill_p50_days":19,"computed_at":"2026-11-10T06:52:35Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Wuxi, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GLP","optional":false},{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-11-03T11:46:37Z","employer_posted_date":"2026-11-03","last_verified_at":"2026-11-10T10:34:01Z","board_verified":true,"closed_at":null,"days_open":7,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":7},"description":"Typical Accountabilities\n主要职责\nSpecific Responsibilities/Tasks\nRoutine work 日常工作\nFinish the routine analytical work accurately and timely\nundefined\nIssue the analytical method transferring and validation protocol for raw materials finish products etc.,\nundefined\nConduct the maintenance and validation for instrument periodically based on plan and keep it in good status.\nundefined\nDouble-checking the BAR.\nundefined\nResponsible for the management of chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory\nundefined\nResponsible for the handling and disposal of lab wasted articles/expire reagent/toxic substances\nundefined\nKeep the chemical lab tidy and clean at any time.\nundefined\nReport any deviation timely, lead major deviation/OOS investigation \nundefined\nStability study management\nundefined\nIssue and revise specification, test method and batch analysis record of starting materials and finished products, and purchasing specification, test method for PQ, CQ etc.\nundefined\nPrepare specification for application (draft) and specification explanation\nundefined\nMaintenance of QC E-system eg. GQCLIMS,1Lab, Empower\n /Empower\nNew employee training\nundefined\nIssue technical assessment report\nundefined\nLead team level CI project\nundefined\nS.H.E. Responsibilities\nSHE 职责\nTake personal responsibility for security to protect themselves and avoid harm to others and the environment\nundefined\nParticipate the necessary security training and drills with the contingency project\nundefined\nStrictly enforce the job safety procedures\nundefined\nReport any incidents , accidents and hazards in work timely\nundefined\nPurchase/ store/ use controlled chemicals.\nundefined\nGMP compliance\nGMP 符合性\nStrictly following SOP and Guideline\n严格执行岗位操作规程和指南\nTake GMP training and strictly following GMP compliance\n参加GMP培训，严格遵守GMP与法规要求\nFill in related documentation such as BAR, other logbook etc., timely to ensure the accuracy of content as per requirement of SOPs.\nundefined\nTake part in actively in correction to the observations found in self-inspection.\n积极参加对自检中所发现缺陷的整改\nTraining and development\n培训和发展\nParticipate actively in serials training required to be held by internal and external.\nundefined\nDevelop all kinds of skills in relation to work field and pursue continuous improvement\n发展各种工作技能并追求持续的改进\nOthers\n其他\nAssist the senior engineer in completing tasks when required.\nundefined\nComplete other tasks arranged according to business needs\n根据业务需要完成安排的其他工作\nQualifications资质\nEducation, Experience and Training\n教育、工作经验和培训\nEducation, Experience and Training\n教育、工作经验和培训\nAcademic / Professional qualification 学历/专业资格\nBachelor or above 本科或以上学历\nTechnical / skills training 技术/技能训练\nBasic GMP, GLP knowledge; Experience in QC 基本的GMP, GLP知识及QC经验\nWorking experience 工作经验 (No. of years / 年 资, Job function /工作功能, Business types /业务种类 )\n- Essential 必需\nMore than 4 years working experience in pharmaceutical company or related industry\n4年以上制药企业或相关行业的工作经验\n- Desirable 理想\nMore than 5 years working experience in pharmaceutical company or related industry\n5年以上制药企业或相关行业的工作经验\nCapabilities\n能力\nLanguage ability/ 语言能力\nFluent English skill in both oral and written\n流利的英文交流和读写能力\nComputer literacy/电脑知识\nGood computer skill 良好的计算机能力\nCommunication ability/ 沟通能力\nGood communication and presentation skills\n良好的沟通和展示技能\nOthers/ 其他\nGood team work spirit 良好的团队合作精神\nSense of responsibility and work actively\n富有责任心及工作积极\nDate Posted\n03-Nov-2026Closing Date\n30-Jan-2027AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. 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