Senior Scientist. Cell Therapy Process Development

AstraZeneca • Gaithersburg, MD

1d • $116,284 - $174,426 • Onsite

About The Position

We are seeking a highly motivated Senior Scientist to lead and execute CAR-T cell therapy process development activities, with an emphasis on autologous manufacturing processes. The successful candidate will apply strong scientific and technical judgment to develop robust, scalable, and transferable processes; evaluate new cell therapy processing equipment; and collaborate across research, analytical, drug product, manufacturing, quality, and regulatory functions to advance programs from preclinical development through clinical stages.

Requirements

• PhD in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biotechnology, Biochemistry, Biological Sciences, Immunology, or a related discipline with at least 1 years of relevant experience; or MS with at least 4 years; or BS with at least 6 years of relevant industry or academic experience.
• Demonstrated experience in cell therapy process development, preferably with autologous CAR-T or other genetically modified immune-cell products.
• Experience leading complex experimental programs and working effectively in a matrixed, cross-functional development environment.
• Strong hands-on experience with mammalian cell culture, aseptic processing, and development of cell therapy manufacturing processes.
• Demonstrated ability to design experiments, analyze complex datasets, draw scientifically sound conclusions, and translate findings into process recommendations.
• Experience with flow cytometry-based instruments and analysis software, including sample preparation, acquisition, gating, data review, and interpretation.
• Experience operating and troubleshooting cell processing equipment and single-use systems used in cell therapy development.
• Working knowledge of process scale-up, technology transfer, process characterization, and manufacturing control strategies.
• Excellent written and verbal communication skills, with the ability to prepare high-quality technical documents and present conclusions to multidisciplinary audiences.
• Ability to work independently, manage multiple priorities, and adapt effectively in a fast-paced development environment.

Nice To Haves

• Direct experience developing autologous CAR-T processes across multiple unit operations and stages of product development.
• Familiarity with available cell therapy processing platforms for cell isolation, washing, concentration, activation, expansion, formulation, and closed-system processing. Experience may include platforms such as CliniMACS Prodigy, Sepax/Sefia, LOVO/CUE, DynaCellect, G-Rex, or comparable systems.
• Advanced flow cytometry experience, including multicolor panel design, compensation or spectral unmixing, gating strategy development, and analysis of T-cell phenotype and functional markers.
• Knowledge of T-cell biology, immunology, cellular engineering, gene delivery technologies, and the relationship between process conditions and product quality attributes.
• Experience supporting GMP manufacturing, process validation, regulatory filings, deviation investigations, and interactions across clinical development stages.
• Experience with automation, digital process monitoring, data visualization, or statistical software used in bioprocess development.
• Demonstrated scientific leadership through mentoring, publications, patents, regulatory contributions, or cross-functional program leadership.

Responsibilities

• Lead the design, execution, and interpretation of laboratory studies supporting CAR-T process development, including cell selection, activation, gene modification, expansion, harvest, formulation, and cryopreservation.
• Develop and optimize unit operations and integrated manufacturing workflows for autologous CAR-T products using quality-by-design and risk-based principles.
• Evaluate, select, and implement commercially available cell therapy process equipment and closed or functionally closed processing technologies; assess fit for intended use, scalability, process robustness, and manufacturing readiness.
• Develop equipment operating strategies, define critical process parameters, and troubleshoot cell processing platforms and associated single-use consumables.
• Apply flow cytometry to characterize cell identity, phenotype, viability, activation, differentiation, and other process-relevant attributes; partner with analytical teams on panel strategy, assay execution, and data interpretation.
• Perform statistical and multivariate data analysis to understand process performance, identify sources of variability, and inform process characterization and control strategies.
• Lead cross-functional technical discussions, communicate study outcomes, and provide clear recommendations to project teams and governance forums.
• Support technology transfer to internal and external GMP manufacturing sites, including process documentation, training, engineering runs, deviation investigations, and manufacturing troubleshooting.
• Author and review development reports, protocols, risk assessments, technical transfer documents, regulatory submission content, scientific publications, and invention disclosures.
• Mentor junior scientists and contribute to a collaborative, safe, and scientifically rigorous laboratory culture.

Benefits

• Competitive remuneration and benefits apply
• Competitive Total Reward program including a market driven base salary, bonus and long-term incentive.
• Generous paid time off program
• Comprehensive benefits package
• Qualified retirement programs
• Paid time off (i.e., vacation, holiday, and leaves)
• Health, dental, and vision coverage in accordance with the terms of the applicable plans.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree