Senior Scientist, Analytical Sciences

Posted 2 Hours Ago
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Santa Monica, CA, USA
In-Office
112K-168K Annually
Senior level
Biotech • Pharmaceutical
The Role
Lead development and qualification of cell-based bioassays and multi-parametric flow cytometry methods for engineered cell therapy product characterization, stability, and release. Provide technical leadership, apply QbD/DOE, transfer methods to QC/external partners, draft regulatory CMC and SOPs, operate laboratory instrumentation, and collaborate with Process Development and Quality teams.
Summary Generated by Built In

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-2026

Closing Date

19-Jul-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.

Skills Required

  • BS/BA in Immunology, Cell Biology, Bioengineering, Analytical Sciences, or related with 5+ years experience; MS/MA with 3+ years; or Ph.D. with no prior industry experience
  • 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
  • Advanced knowledge in T cell biology and cell signaling pathways
  • Proficiency with Microsoft Excel, Word, PowerPoint and data analysis software (e.g., Prism, JMP, FlowJo, CytExpert, SoftMax Pro)
  • Ability to think critically with strong troubleshooting and problem-solving skills
  • Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside initial job description
  • Experience working in a fast-paced laboratory environment with moderate direction and supervision
  • Extensive hands-on experience executing assays and analyzing multi-color flow cytometry data (10+ colors)
  • Knowledge of QbD approaches to analytical method development including gap and risk assessments, DOE and statistical analysis

AstraZeneca Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.

  • Fair & Transparent Compensation Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
  • Strong & Reliable Incentives Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
  • Retirement Support A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.

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The Company
HQ: Gaithersburg, MD
70,000 Employees
Year Founded: 1999

What We Do

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.

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