Process Engineer, Cell Therapy Process Development job opportunity at AstraZeneca.



DatePosted 30+ Days Ago bot
AstraZeneca Process Engineer, Cell Therapy Process Development
Experience: 3-years
Pattern: full-time
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Cell Therapy Process Development

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loacation US – Santa Monica Colorado Avenue – CA, United States Of America
loacation US – Santa Mon..........United States Of America

We are   seeking   a highly motivated   Process   Engineer to support   late-stage   cell therapy   process   development and   characterization activities. In this role, you We are seeking   a highly motivated Process Engineer to support late-stage cell therapy process development and characterization activities. In this role, you will play critical role in advancing late-stage cell therapy process development, process characterization, and BLA‑enabling studies.     This position focuses specifically on cell therapy unit operations, including T-cell enrichment, activation, transduction,   washes   and harvest either semi-automated or   fully   automated equipment.    The ideal candidate brings deep technical   expertise , hands-on experience with cell therapy unit operations, and   demonstrates   success in supporting clinical and commercial readiness.   Key Responsibilities   Process development and   characterization   Design, execute, and support autologous or allogenic cell therapy process optimization and robustness studies .     Drive implementation of closed-system operations and automation strategies to support scalability and compliance.    Plan and execute process characterization studies (DOE, multivariate studies, scale‑down models, and scale‑up assessments) in alignment with QbD and ICH guidelines .   Perform data analysis,   write technical report s , and present outcome of the studies to cross‑functional teams and governance forums.   Conduct batch record review, deviation assessment, and data trending to ensure robustness of cell therapy manufacturing processes.   Apply AI‑enabled tools and digital analytics to accelerate data review, trend analysis, batch record evaluation, and process understanding.   PPQ, Tech Transfer & Manufacturing Readiness   Provide on‑the‑floor technical support during scale‑up, engineering runs, PPQ batches, and commercial manufacturing campaigns (including off‑shift support when   required ).   Support raw material risk assessments, comparability studies, and process risk evaluations across facilities and platforms.   Cross‑Functional Collaboration   Work closely with analytical sciences and manufacturing science and technology teams to ensure end‑to‑end process alignment.   Support lifecycle management, post‑approval changes, and continuous improvement initiatives for   cell therapy processes.   Qualifications   B.S. in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field with 3+ years of hands‑on industry experience; OR M.S. with 2+ years; OR Ph.D. with 0 years of industry experience  Strong technical expertise in key cell therapy unit operations (e.g., cell isolation, activation, transduction, expansion, harvest, formulation, cryopreservation) or biologics .   Demonstrated experience with GMP operations and late‑stage / commercial readiness.   Proven ability to analyze complex datasets, develop sound recommendations, and communicate clearly across levels   Experience with late‑stage development and process characterization principles for   cell therapy processes.   Demonstrated proficiency in applying AI tools and digital solutions to data analysis, documentation, and workflow automation.   Experience working in GMP environments, including batch record execution or review, deviations, and investigations.   Strong technical writing, data analysis, and problem‑solving skills.   Familiarity with automation platforms (e.g.,   CliniMACS   Prodigy, Lovo, G-Rex, Wave bioreactors).   Experience implementing closed, automated, or high‑throughput systems.   Experience designing and executing DOE and multivariate data analysis for   cell therapy   processes.   Experience with JMP or similar statistical analysis tools.   Formal training or demonstrated application of digitalization, automation, or AI‑enabled tools in bioprocess development.   The annual base pay for this position ranges from $79,336 to $119,005 . 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. Date Posted 29-Jan-2026 Closing Date 18-Feb-2026 Our 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. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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