Associate Process Engineer, Cell Therapy Process Development

Position Summary  We are seeking a highly motivated Associate 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.Brings 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 reports, 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.  Required Qualifications  • B.S.  in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field; OR associate degree. with 2+ years hands‑on 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.  Preferred Qualifications   • 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.  Key Competencies  • Experimental design and execution skills.  • Cross‑functional communication and collaboration.  • Ability to operate effectively in fast‑paced, late‑stage development environments.  • Scientific curiosity, ownership mindset, and willingness to support manufacturing operations.  The annual base pay for this position ranges from $67K to $101K. Our positions offer eligibility for multiple 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 t