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8 дней назад

Scientist, In Vivo High Throughput Screening & Analytics

133 195 - 172 370$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Scientist, In Vivo High Throughput Screening & Analytics (biotechnology and cell/gene therapy): Designing and executing high-throughput screening, automated assay, vector characterization, and data analysis workflows for in vivo lentiviral vector research with an accent on reproducibility, analytical rigor, and cross-functional scientific decision-making. Focus on optimizing liquid-handling workflows, interpreting complex cell- and vector-based assay data, and solving automation, assay variability, and data integrity challenges.

Location: Philadelphia, Pennsylvania, United States

Salary: $133,195–$172,370 per year, plus potential annual bonus, stock-based long-term incentives, paid time off, and benefits.

Company

hirify.global is a biopharmaceutical company developing cancer immunotherapies, including CAR T-cell and T-cell receptor engineered therapies.

What you will do

  • Design, plan, and execute high-throughput screening, miniaturized, scale-down, and analytical experiments for lentiviral vector research.
  • Develop, optimize, and troubleshoot automated and semi-automated laboratory workflows using liquid handling, scheduling, plate-based assay, and data capture platforms.
  • Execute and analyze mammalian cell-, vector-, and analytical assays covering transduction, binding, expression, potency, and vector performance.
  • Build data reduction, visualization, quality control, and reporting workflows using tools such as Python, R, SQL, VBA, JMP, Prism, and Spotfire.
  • Interpret complex experimental data, recommend evidence-based next steps, and communicate findings through technical reports, presentations, and data packages.
  • Collaborate with Discovery, Process Development, Analytical Development, and other research functions while maintaining traceable records and training colleagues.

Requirements

  • MS with 4+ years of relevant experience, BS with 6+ years, or PhD/PharmD in a relevant scientific discipline with applicable experience.
  • Advanced knowledge of biotechnology, molecular biology, cell biology, immunology, biomedical engineering, analytical development, or a related field.
  • Experience with high-throughput screening, assay miniaturization, laboratory automation, automated liquid handling, or scale-down systems.
  • Hands-on experience with mammalian cell culture, plate-based assays, vector or cell-based characterization, and analytical method development.
  • Ability to independently design experiments, troubleshoot methods, analyze complex data, define next steps, and communicate scientific findings.
  • Strong documentation, data quality, laboratory safety, reproducibility, collaboration, and mentoring skills.

Nice to have

  • Experience with lentiviral vector production, primary immune cell or T-cell assays, transduction, flow cytometry, ELISA/AlphaLISA, BLI/Octet, internalization, or potency assays.
  • Experience with Tecan, Hamilton, Beckman Biomek, CyBio FeliX, Opentrons, or comparable laboratory automation platforms.
  • Programming or scripting experience in Python, R, SQL, VBA, MATLAB, or related tools.
  • Familiarity with Design of Experiments, multivariate optimization, assay qualification, and statistical methods.

Culture & Benefits

  • Full-time employment within a cross-functional cancer immunotherapy research organization.
  • Medical, dental, vision, and life insurance plans.
  • Paid time off and potential discretionary annual bonus.
  • Potential eligibility for discretionary stock-based long-term incentives.
  • Inclusive environment focused on employee development, collaboration, and scientific impact.

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