Senior Scientist, Analytical Sciences
We are seeking a collaborative and technical Senior Scientist experienced in cell culture, immunological techniques, multi-parametric flow cytometry and cell-based functional assays as part of bioassay development. The individual will deliver new/optimized analytical methods and evaluate new analytical technologies. The candidate will be responsible to develop cell-based analytical methods aligned with vector and cellular therapy product CQAs to enable process development, product characterization, stability and release testing of novel engineered cell therapy products. The Senior Scientist will work extensively with the Process Development and Quality Control teams. This role is based out of Santa Monica, CA and reports directly to the Director, Product Analytical Sciences.
Responsibilities
Provide strategic, technical, and scientific leadership to a highly technical analytical method development team, assign duties, review data, and reinforce regulatory concepts (cGMP).
Responsible to advance and implement cell-based bioassay/potency (e.g. cytotoxicity, proliferation, cytokine production) and immunophenotyping by multi-parametric flow cytometry methods from conception through optimization, qualification, and method transfer to Quality Control and/or external partners as part of an analytical control strategy and in support of Process Development.
Employ quality by design (QbD) and design of experiment (DOE) approaches to method development to quickly identify robust operating regions within phase-appropriate pre-defined acceptance criteria aimed to meet ICH guidelines.
Work with Process Development, executing and documenting analytical methods as part of experimental study plans to progress and characterize novel engineered cell therapy platforms, and occasionally perform routine assays for characterization.
Work cross-functionally with Quality partners during technology transfers, assist in drafting qualification/validation protocols/reports.
Write, review and edit accurate technical and development reports, CMC sections for regulatory submissions, and SOP/maintenance/user requirements for relevant equipment
Participate in group and department meetings, present scientific data, provide expertise in areas of responsibility.
Maintain, calibrate and operate analytical equipment and instrumentation that is used routinely in execution of assays.
Required Qualifications and Skills
BS/BA in Immunology, Cell Biology, Bioengineering, Analytical Sciences, or a related discipline with 5+ years of relevant hands‑on experience or MS/MA with 3+ years of relevant experience or Ph.D. with no prior industry experience
Demonstrate knowledge of Process Development of cellular therapy products and Analytical Method Development within a regulated environment
First-hand experience in development and qualification of immunoassays, multi-parameter flow cytometry, and cell-based potency methods for release in a QC/regulated environment
Demonstrate advanced knowledge in T cell biology and cell signaling pathways
Excellent skills in Microsoft Excel, Word and PowerPoint and data analysis software (e.g. Prism, JMP, FlowJo, CytEpert, SoftMax Pro)
Ability to think critically and demonstrate troubleshooting and problem-solving skills.
Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description.
Experience and aptitude in working in a fast-paced laboratory environment with moderate direction and supervision.
Preferred skills
Extensive hands-on experience in executing assays and analyzing data using multi-color flow cytometry (10+ colors).
Demonstrate knowledge of QbD approaches to analytical method development including gap and risk assessments, DOE and statistical analysis.
#CellTherapy
The annual base pay for this position ranges from $112K to $168K. 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
10-Jul-2026Closing Date
19-Jul-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. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
AstraZeneca 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. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.
Gå med i vårt talangnätverk
Bli först med att få jobbuppdateringar och nyheter från AstraZeneca
Registrera