{"id":3354580,"url":"https://alion.io/job/astrazeneca-quality-control-specialist","title":"Quality Control Specialist","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":93,"open_postings":165,"ghost_share":0.006,"stale_share":0.388,"repost_share":0.103,"time_to_fill_p50_days":19,"computed_at":"2026-11-05T05:54:30Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Los Angeles, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":80910,"max":121364,"currency":"USD","period":"year","gross":null,"usd_annual":121364},"salary_estimate":null,"experience_years_min":4,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Cell Culture","optional":false},{"name":"ELISA","optional":false},{"name":"Flow Cytometry","optional":false},{"name":"qPCR","optional":false}],"status":"closed","first_seen_at":"2026-10-27T19:35:23Z","employer_posted_date":"2026-10-27","last_verified_at":"2026-11-04T10:54:37Z","board_verified":false,"closed_at":"2026-11-04T10:54:37Z","days_open":7,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":7},"description":"Quality Control Specialist\nIntroduction to role\nAre you driven to ensure cell therapy products meet the highest standards and reach patients without delay? Do you see yourself using rigorous analytical science to accelerate safe, effective treatments to those who need them most? Join our Quality Control team and take on a high-visibility role where your decisions and data will directly influence product release and stability strategies.\nIn this role, you will be a key contributor to advancing our cell therapy pipeline, owning analytical method qualification and executing critical testing that underpins lot release and in-process control. You will organize, analyze, and present results with clarity, ensuring the QC Analytical laboratory runs reliably and compliantly. Your expertise will be recognized across teams, and your voice will help shape how we deliver consistently high-quality outcomes for patients.\nAccountabilities\nRelease and Stability Testing: Perform flow cytometry, ELISA, cellular cytotoxicity, dPCR, and cell-based potency assays to enable timely release testing and stability monitoring of cell therapy products and in-process samples, ensuring data integrity and fit-for-purpose results.\nAnalytical Method Lifecycle: Support analytical method development, qualification, and technical transfer from Analytical Development; design, execute, and document qualification activities to ensure robust, reproducible methods ready for routine use.\nTechnical Leadership and SME Support: Serve as a subject matter expert in technical discussions, document reviews, and investigations; provide data-driven guidance that resolves issues quickly and prevents recurrence.\nDocumentation and Compliance: Author and/or review analytical test results, analytical study data summaries and reports, analytical method qualification protocols and reports, and standard operating procedures, ensuring alignment with regulatory expectations and internal quality standards.\nRoutine Operations Excellence: Support daily QC analytical activities, monitor lab performance, and ensure the laboratory operates as expected, including occasional off-hour or weekend technical support to meet lot release timelines.\nMentoring and Knowledge Sharing: Mentor and train associate specialists, elevating team capability and building consistent analytical practice across the laboratory.\nContinuous Improvement and Broader Impact: Identify opportunities to streamline workflows, improve assay performance, and reduce cycle time; translate scientific insights into operational gains that enhance product quality and speed to patients.\nEssential Skills/Experience\nAssociate’s degree in biological sciences or related field with 4+ years of experience, Bachelor’s degree in biological sciences or related field with 2+ years of experience, or MS in biological sciences or related field with 0+ years of experience is required.\nFlexibility of occasionally working on weekends or holidays to support lot release testing.\nDemonstrated ability to take ownership, initiative, and self-accountability.\nDemonstrated ability to collaborate, work, and communicate effectively across organizational interfaces in a fast-paced dynamic team setting.\nAttention to detail and quick learning/application of concepts and information.\nKnowledge of cell culture techniques and proficient in MS Word, Excel, Power Point and other applications.\nAbility to communicate and work in a self-guided manner with scientific/technical personnel.\nWell-versed in various analytical techniques Flow cytometry, qPCR, dPCR, cell-based potency and/or ELISA experience.\nDesirable Skills/Experience\n2+ years of relevant experience in the Pharmaceutical or Biotechnology industry.\nExperience in Cell or Gene Therapy.\nWell-versed in various analytical techniques such as Flow cytometry, qPCR, dPCR, cell-based potency and/or ELISA experience.\nWhy AstraZeneca\nHere, scientific rigor meets real-world impact. You will work alongside specialists who bring diverse perspectives into the same room to unleash bold thinking, applying advanced analytics and modern lab technologies to decisions that put patients first. Your contributions are visible and valued, with opportunities to stretch your skills across functions, learn from peers, and take on meaningful responsibility. We value kindness alongside ambition, support curiosity, and recognize progress-even when it comes through constructive challenge-so you can grow while making a measurable difference in the lives of patients worldwide.\nIf you are ready to turn your analytical expertise into outcomes that release therapies faster and safer, step into this role and help shape the future of cell therapy quality today.\nThe annual base pay for this position ranges from $80,910 to $121,364. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.\nDate Posted\n27-Oct-2026Closing Date\n02-Nov-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. 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