Clinical Laboratory Scientist: Molecular Diagnostics & R&D

Mindera Health

Vista (CA)

On-site

USD 105,000 - 120,000

Full time

15 hours ago
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Benefits offered by this job

Stock options
Performance bonus

Job summary

Mindera Health in Vista, CA is seeking a Clinical Laboratory Scientist for a full-time, on-site role in our CAP/CLIA-certified laboratory. You will perform high complexity molecular testing, including DNA/RNA extraction and qPCR, align with safety and regulatory standards.

The role requires a Bachelor's degree in biology and state licenses (CLS or CGMBS); ASCP Molecular Biology certification is preferred. You will calibrate equipment, run QC, document results, and contribute to assay development

Qualifications

  • Bachelor’s degree in biology or related field is required.
  • California CLS or CGMBS license is required.
  • ASCP Molecular Biology certification preferred.
  • Minimum of 1 year in a clinical molecular lab preferred.

Responsibilities

  • Performs daily routine and complex molecular tests (DNA/RNA extraction, qPCR, NGS).
  • Maintains reagent and consumable inventory and quality control.
  • Reviews test results and documents procedures per SOPs.
  • Troubleshoots technical and non-technical issues and participates in proficiency testing.
  • Maintains records to ensure regulatory compliance and participates in assay improvements.

Skills

Molecular biology
DNA probes design
Analytical skills
Communication skills
Team collaboration

Education

Bachelor's degree in biology
California CLS license
CGMBS license
ASCP Molecular Biology

Job description

Mindera Health in Vista, CA is seeking a Clinical Laboratory Scientist for a full-time, on-site role in our CAP/CLIA-certified laboratory. You will perform high complexity molecular testing, including DNA/RNA extraction and qPCR, align with safety and regulatory standards.

The role requires a Bachelor's degree in biology and state licenses (CLS or CGMBS); ASCP Molecular Biology certification is preferred. You will calibrate equipment, run QC, document results, and contribute to assay development

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