Molecular Quality Assurance Technician

NeoGenomics

Aliso Viejo (CA)

On-site

USD 55,000 - 75,000

Full time

14 days+
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Benefits offered by this job

Tuition reimbursement
401k match
Employee Stock Purchase Plan
Paid time off / 16 days + holidays
Wellness programs

Job summary

NeoGenomics in Aliso Viejo, CA is seeking a Quality Specialist Technician for the Molecular department to drive quality initiatives and ensure GLP/regulatory compliance across operations.

The role emphasizes maintaining records, supporting CAP/FDA/CLIA readiness, and collaborating with QA and Compliance to sustain a robust quality program. Shift is 10:00am-6:30pm, Sunday-Thursday or Tuesday-Saturday, with ongoing training and career development opportunities.

Qualifications

  • Bachelor’s degree in chemical, physical, or biological sciences required.
  • At least one year of laboratory experience or training.
  • Molecular-based testing experience preferred.
  • Experience in Laboratory Quality Program preferred.

Responsibilities

  • Maintains awareness of and ensures compliance with regulatory guidelines (CAP, FDA, CLIA, HIPAA, OIG, OSHA, CMS).
  • Manages area specific to quality control and regulatory requirements (SOPs, proficiency testing, calibration verification, competency).
  • Coordinates quality control activities and monitors adherence to QC measures.
  • Analyzes data to detect trends and deviations; develops corrective actions and follow-ups.
  • Maintains digital and physical records including training/competency files and QC documentation.
  • Supports sample storage coordination with Laboratory and Banking departments.

Skills

Laboratory experience
Quality program experience
Molecular testing exposure

Education

Bachelor’s degree in chemical/physical/biological sciences

Job description

NeoGenomics in Aliso Viejo, CA is seeking a Quality Specialist Technician for the Molecular department to drive quality initiatives and ensure GLP/regulatory compliance across operations.

The role emphasizes maintaining records, supporting CAP/FDA/CLIA readiness, and collaborating with QA and Compliance to sustain a robust quality program. Shift is 10:00am-6:30pm, Sunday-Thursday or Tuesday-Saturday, with ongoing training and career development opportunities.

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