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2 дня назад

Scientist I (NGS/MRD)

130 000 - 140 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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 I (NGS/MRD): Developing and implementing next-generation sequencing-based minimal residual disease assays for cancer diagnostics with an accent on molecular biology, assay optimization, and clinical laboratory workflows. Focus on designing and analyzing feasibility and validation studies, troubleshooting experimental workflows, and transferring assays into regulated clinical laboratory environments.

Location: Onsite in South San Francisco, California, United States

Salary: $130,000–$140,000 USD per year

Company

hirify.global is a diagnostics company developing genomic and clinical-data-driven cancer tests supported by bioinformatics, AI, and evidence generation.

What you will do

  • Support the development, optimization, verification, and transfer of NGS-based MRD assays from feasibility through clinical laboratory implementation.
  • Execute and analyze feasibility, characterization, optimization, and pre-validation studies.
  • Prepare and characterize clinical and contrived samples for assay development and validation.
  • Design experiments, interpret results, troubleshoot workflows, and implement technical improvements.
  • Develop and optimize automated high-throughput laboratory workflows.
  • Collaborate with Bioinformatics, Data Science, Operations, Clinical Laboratory, Automation, Quality, Regulatory, and Software/LIMS teams.

Requirements

  • Ph.D. in Molecular Biology, Genetics, Biochemistry, Cancer Biology, or a related field.
  • At least 3 years of relevant industry or postdoctoral experience in molecular diagnostics, biotechnology, genomics, or a related field.
  • Hands-on experience with NGS workflows, library preparation, DNA- and/or RNA-based assays, and NGS quality control methods.
  • Experience with experimental design, laboratory execution, data analysis, interpretation, troubleshooting, and assay optimization.
  • Familiarity with statistical analysis and data visualization tools such as JMP, R, or Python.
  • Must work onsite in South San Francisco, California, United States.

Nice to have

  • Experience with blood, plasma, tissue, or FFPE clinical samples.
  • Exposure to CAP/CLIA, NYSDOH, design control, or other regulated product development environments.
  • Experience with oncology, liquid biopsy, ctDNA, or MRD technologies.

Culture & Benefits

  • Purpose-driven work focused on improving cancer patient outcomes.
  • Collaborative, multidisciplinary product development environment.
  • Competitive compensation, discretionary bonus or incentive eligibility, and restricted stock units.
  • Inclusive workplace with opportunities for professional growth.
  • Employment in a company recognized as a 2024 Certified Great Place to Work in the United States and Israel.

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