High-Throughput NGS Assay Scientist I

Fulgent Therapeutics LLC

El Monte (CA)

On-site

USD 85,000 - 106,000

Full time

13 days ago
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Job summary

Fulgent Therapeutics LLC is seeking an Assay Development Research Scientist I to design and develop automated, high-throughput NGS-based genetic tests from concept through commercial launch. The role emphasizes collaboration, cross-functional projects, and integration of cutting-edge tech within the lab.

The candidate will contribute to test development, troubleshooting, and maintaining existing assays while ensuring compliance with CLIA/CAP and HIPAA standards in a dynamic biotech environment

Qualifications

  • PhD or Master's Degree in Molecular Biology, Biochemistry, Genetics, or related field. >3 yrs for PhD; >5 yrs for MS preferred.
  • Experience with DNA/RNA library prep, Target amplification, and NGS.
  • Knowledge of human genetics, NGS, and genotyping.
  • Prior CLIA/CAP lab and genetic company experience preferred.
  • Basic bioinformatics understanding; HIPAA and SOP familiarity.

Responsibilities

  • Develop scaled, high-sensitivity NGS tests from concept to launch.
  • Design and optimize genetic assays and evaluate sequencing technologies.
  • Troubleshoot Illumina sequencing platforms and automated lab workflows.
  • Analyze data, communicate results clearly to cross-functional teams.
  • Ensure quality control of algorithms and panel updates.

Skills

Genetics/molecular biology experience
Attention to detail
Independent and collaborative work
Regulatory awareness (HIPAA)
Communication of results

Education

PhD or MS in Molecular Biology/Genetics

Tools

Illumina sequencing instruments
Bioinformatics basics

Job description

Fulgent Therapeutics LLC is seeking an Assay Development Research Scientist I to design and develop automated, high-throughput NGS-based genetic tests from concept through commercial launch. The role emphasizes collaboration, cross-functional projects, and integration of cutting-edge tech within the lab.

The candidate will contribute to test development, troubleshooting, and maintaining existing assays while ensuring compliance with CLIA/CAP and HIPAA standards in a dynamic biotech environment

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