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PCR Laboratory Technician

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Rocky Mountain Laboratories
Full Time position
Listed on 2026-07-01
Job specializations:
  • Healthcare
    Medical Technologist & Lab Technician, Clinical Research
Salary/Wage Range or Industry Benchmark: 22 - 27 USD Hourly USD 22.00 27.00 HOUR
Job Description & How to Apply Below

Molecular Laboratory Technician

Rocky Mountain Laboratories – Austin, TX

About Us

Rocky Mountain Laboratories is a clinical laboratory providing comprehensive laboratory services. We are dedicated to delivering accurate and timely diagnostic information and are committed to improving healthcare outcomes through cutting‑edge technology and a customer‑focused approach.

Position

We are seeking a Molecular Laboratory Technician to join our Austin clinical laboratory team. This role is best suited for a technician with recent (within the past 12 months), hands‑on molecular experience in a CLIA‑regulated diagnostic laboratory
.

The ideal candidate has independently performed full molecular workflows on human clinical diagnostic specimens
, including manual nucleic acid extraction, PCR setup, data analysis, and result reporting, and can integrate quickly with minimal ramp‑up time.

Research‑only or academic laboratory experience does not meet the clinical bench requirements for this role.

Schedule:

Tuesdays to Saturdays 10:30 am to 7 pm

Pay: $22–$27/hour, DOE (set by hiring manager)

Responsibilities
  • Perform molecular testing (PCR, RT-PCR, qPCR, and/or NGS) on human clinical specimens in a CLIA‑regulated laboratory environment, including infectious disease and/or genetic testing panels
  • Independently perform full molecular workflows, including specimen accessioning/plating, manual nucleic acid extraction, PCR setup, data analysis, and result reporting
  • Process and manage moderate‑to‑high‑volume daily specimen workflows while maintaining accuracy and turnaround times
  • Prepare reagents, controls, and samples with strict adherence to quality standards
  • Set up, run, and troubleshoot real‑time PCR assays and ensure accurate result interpretation
  • Demonstrate clear understanding of PCR workflow steps and quality checkpoints
  • Record, analyze, and interpret test results; promptly report abnormalities
  • Maintain, calibrate, and troubleshoot laboratory instruments and equipment
  • Operate molecular laboratory instrumentation and systems, including real‑time PCR platforms (Quant Studio 5/6/12), King Fisher Flex extraction systems, and related molecular lab equipment
  • Perform quality control and proficiency testing
  • Ensure compliance with CLIA, CAP, and other regulatory requirements
  • Maintain organized documentation for audits and inspections
  • Prioritize tasks to meet turnaround times in a moderate‑to‑high‑volume clinical environment
  • Collaborate with lab staff and communicate testing updates and issues
  • Maintain a clean and safe laboratory workspace
  • Assist with training of new or temporary staff as needed
  • Support internal audits, continuous improvement initiatives, and special projects as assigned
Required Qualifications

Candidates must meet CLIA requirements for high‑complexity testing personnel (42 CFR 493.1489):

  • Bachelor’s, master’s, or doctoral degree in chemical, physical, biological, or clinical laboratory science, or medical technology
  • OR Associate degree in laboratory science or medical laboratory technology
  • OR 60 semester hours (with at least 24 in biology and chemistry) plus documented training in molecular biology (minimum 3 months) or an accredited clinical laboratory program

(Degrees in non‑laboratory fields at any level are not accepted)

Additional Requirements
  • Minimum 1 year of recent hands‑on experience performing molecular testing on human clinical diagnostic specimens in a CLIA‑regulated laboratory
  • Minimum 6 months of independent manual nucleic acid extraction experience within the past 12 months
  • Demonstrated ownership of full molecular workflows, including specimen preparation/plating, manual nucleic acid extraction, PCR setup, data analysis, and result reporting
  • Experience setting up and resulting real‑time PCR assays (qPCR)
  • Ability to clearly articulate hands‑on bench responsibilities and workflow steps during interview
  • Demonstrated ability to follow protocols and perform high‑complexity testing under CLIA
  • Ability to work independently with minimal supervision after onboarding
  • Strong attention to detail and consistency
  • Reliable and punctual with strong time management skills
  • Proficiency with Microsoft Office and computer‑based data entry
  • Clear…
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