K

Kite Pharma

Develops engineered T cell cancer therapies

Scientist – RNA Biology

Translational Research & Bench BiologyConfirmed live in the last 24 hours
Full-timeFoster City, CA, USA

About the Job

Requirements

  • A doctorate in Molecular Biology, Biochemistry, Chemical Biology, Bioengineering, Pharmaceutical Sciences, RNA Biology, or a related field; or a master's degree in a relevant scientific discipline with at least four years of relevant experience; or a bachelor's degree in a relevant scientific discipline with at least six years of relevant experience.
  • A doctorate in Molecular Biology, Biochemistry, Chemical Biology, Bioengineering, Pharmaceutical Sciences, RNA Biology, or a related field, with at least three years of relevant industry and/or postdoctoral experience, is preferred.
  • Demonstrated experience applying RNA payload expertise within lipid nanoparticle formulation, encapsulation, or another nucleic acid delivery platform.
  • Depth in one or more advanced RNA areas, such as circular or self-amplifying RNA, modified nucleotides, cap chemistry, untranslated-region engineering, RNA structure, or innate immune sensing.
  • Experience scaling or automating RNA production and purification workflows using chromatography, tangential-flow filtration, design of experiments, or related process-development approaches.
  • Experience establishing specifications, reference standards, qualified assays, method-transfer packages, or comparability strategies for research-stage RNA products.
  • Ability to connect RNA critical quality attributes with cell-based expression, potency, tolerability, or durability readouts.
  • Experience supporting cell therapy, in vivo cell engineering, oncology, or other cancer-focused research programs.
  • Evidence of scientific impact through publications, patents, technology development, or leadership of an RNA therapeutics, drug-delivery, or molecular-engineering platform.

Responsibilities

  • Own end-to-end research-scale RNA production, including DNA template preparation, in vitro transcription, capping, polyadenylation or encoded poly(A) strategies, purification, concentration, buffer exchange, sterile handling, and storage.
  • Develop, optimize, and standardize workflows for linear mRNA, while expanding capabilities for circular RNA, self-amplifying RNA, and other emerging RNA formats as program needs evolve.
  • Design and evaluate RNA sequence and chemistry variables, including untranslated regions, coding-sequence optimization, poly(A) architecture, cap structures, and modified nucleotides, to improve expression, stability, and tolerability.
  • Establish fit-for-purpose RNA quality-control methods and acceptance criteria for identity, concentration, purity, integrity, size distribution, capping efficiency, poly(A) characteristics, residual DNA, double-stranded RNA, endotoxin, bioburden where appropriate, and functional activity.
  • Operate, maintain, qualify, and troubleshoot research instruments used for RNA production and analysis, including liquid-handling systems, chromatography and tangential-flow filtration platforms, capillary electrophoresis, high-performance liquid chromatography, spectrophotometry, fluorometric assays, and quantitative or digital PCR systems.
  • Partner closely with lipid nanoparticle formulation scientists to define RNA input specifications, assess compatibility with formulation processes, support RNA encapsulation, and determine how payload quality affects encapsulation efficiency, particle attributes, expression, and biological activity.
  • Develop data packages and documentation that enable comparability across RNA lots, constructs, production methods, and lipid nanoparticle formulations.
  • Lead investigations of failed or variable RNA and lipid nanoparticle experiments, identify root causes, and implement corrective actions and process improvements.
  • Independently generate hypotheses, design experiments, analyze results, and recommend clear next steps for platform and program teams.
  • Collaborate with molecular biologists, cell biologists, formulation scientists, analytical scientists, automation experts, and in vivo teams to advance RNA-lipid nanoparticle programs for cancer therapies.
  • Maintain rigorous electronic records, methods, reagent inventories, instrument logs, and safe laboratory practices; contribute to scalable and transferable workflows.
  • Mentor junior scientists and serve as a technical resource for RNA design, manufacturing, analytics, and troubleshooting.

Desired Qualifications

  • Strong communication, collaboration, and problem-solving skills, with the ability to work effectively in multidisciplinary teams.

About the Company

Kite Pharma

Develops engineered T cell cancer therapies

Kite Pharma develops cancer immunotherapies by engineering a patient’s own T cells to attack tumors. Its core product strategy centers on cell therapy where T cells are genetically modified to recognize cancer cells, expanded outside the body, and then infused back into the patient to destroy cancer. This approach differs from traditional drugs by using the immune system itself to fight cancer and by tailoring therapies to individual patients. Kite focuses on clinical trials and commercialization of approved therapies, often through partnerships and licensing with other pharmaceutical companies to reach patients worldwide. The company’s goal is to provide potentially lifesaving, durable cancer treatments and move toward a cure for cancer.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Santa Monica, CA
Founded
2009

Recently Posted Jobs

Explore more opportunities at Kite Pharma

See more jobs