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1110 Kite Pharma, Inc. Verified 7h ago

Scientist, Method Automation

United States - California - Santa Monica On-site

$133,195–$172,370 a year
Pay$133,195–$172,370
TypeFull-time
Work settingOn-site
Verified listing

JobFig found this opening at its original source and checks that it remains available.

About the role

Everyone at Kite is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Join us in this mission!Everyone at Kite is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Join us in this mission! We are seeking a motivated Scientist, Method Automation to support automated and process analytical technology (PAT)-enabled analytical workflows within Analytical Development. This role will contribute to method automation, assay workflow optimization, technology evaluations, and data-rich testing approaches that improve efficiency, reproducibility, data integrity, and transfer readiness. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary.

What you'll bring

  • or
  • PhD 0+ years of relevant experience in analytical development, method development, method automation, bioassay development, or a related biopharmaceutical laboratory environment.
  • MS with 4+ years of relevant experience in analytical development, method development, method automation, bioassay development, or a related biopharmaceutical laboratory environment.
  • BS with 6+ years of relevant experience in analytical development, method development, method automation, bioassay development, or a related biopharmaceutical laboratory environment.
  • PhD 3+ years of relevant experience in analytical development, method development, method automation, bioassay development, or a related biopharmaceutical laboratory environment.
  • MS with 6+ years of relevant experience in analytical development, method development, method automation, bioassay development, or a related biopharmaceutical laboratory environment.
  • BS with 8+ years of relevant experience in analytical development, method development, method automation, bioassay development, or a related biopharmaceutical laboratory environment.
  • Experience with liquid handling or automation platforms such as Hamilton, TECAN, Biomek, Integra, or comparable systems.
  • Experience with high-throughput assays, analytical method lifecycle activities, QC transfer, or regulated method execution.
  • Exposure to PAT, digital laboratory integration, LIMS, ELN, structured data systems, instrument connectivity, electronic batch records, or analytics platforms.
  • Experience with design of experiments, data-rich experimentation, automation scripting, Python, multivariate analysis, machine learning, or comparable tools.
  • Working knowledge of GMP, ALCOA+, 21 CFR Part 11, ICH guidance, regulated documentation, investigations, deviations, change controls, or transfer practices.

Benefits

Life Insurance