Clinical Laboratory Technologist
BioPhase, Seattle, WA, United States
Schedule: M–F, 2:30 pm–11 pm (fully onsite)
Comp: $30 - $55/hr
About the role
Join a high-volume clinical genomics team processing patient and research specimens through next-generation sequencing workflows. You'll run DNA extraction, PCR amplification, and library prep on liquid-handling automation platforms, with results flowing directly to oncologists, clinicians, and research partners. Our laboratories operate under CLIA, CAP, NYS, and FDA frameworks — regulatory precision is built into everything we do.
Day-to-day responsibilities
Execute DNA extraction, PCR, and high-throughput sequencing protocols within a compliant QMS
Operate liquid-handling robotics and next-generation sequencers; perform routine maintenance and troubleshooting
Complete assigned runs—clinical specimens, reagent QC batches, validation studies, and special projects—accurately and on schedule
Log non-conformances, enter run data into the LIMS, and maintain documentation to Good Documentation Practice standards
Uphold GxP, GMP, GCP, and GLP requirements; fulfill high-complexity testing personnel obligations under 42 CFR 493.1495
Maintain continuing education credits required by applicable regulatory bodies
Handle human biological specimens and biohazardous materials according to established safety protocols
Seniority levels
(Level I)
Performs protocols with some supervisory guidance; escalates issues to lead or supervisor
Resolves routine and occasional novel process variations using up-to-date information
Communicates clearly during shift handoffs; keeps detailed records
May provide informal guidance to newer colleagues
(Level II)
Works with minimal direction; exercises considerable clinical initiative
Conducts training and competency evaluations for technician-level staff on high-complexity methods
Proposes procedural improvements to enhance team efficiency; understands when to upscale quality or timeline concerns
(Level III)
Operates independently; regularly applies educated discretion in decision-making
Drives process change recommendations backed by cross-functional knowledge
Proficient in laboratory automation and recognized for best-practice leadership
Qualifications
(Level I) — must meet one of the following
Bachelor's degree or higher in medical technology or laboratory science, or
Bachelor's degree or higher in a chemical or biological science
plus
at least 6 months of high-complexity molecular experience in a CLIA-certified laboratory
(Level II) — must meet all of the following
Bachelor's degree or higher in a relevant science or laboratory science field
Minimum 1 year of clinical lab experience in a high-complexity CLIA setting (or 2 years with a Master's degree or higher)
Minimum 3 years of hands-on molecular laboratory experience (or 2 years with a Master's or higher)
(Level III) — must meet all of the following
Bachelor's degree or higher in a relevant science or laboratory science field
Minimum 3 years of clinical lab experience in a high-complexity CLIA setting (or 2 years with a Master's degree or higher)
Minimum 5 years of molecular laboratory experience (or 3 years with a Master's or higher)
Demonstrated proficiency in laboratory automation and best practices
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Comp: $30 - $55/hr
About the role
Join a high-volume clinical genomics team processing patient and research specimens through next-generation sequencing workflows. You'll run DNA extraction, PCR amplification, and library prep on liquid-handling automation platforms, with results flowing directly to oncologists, clinicians, and research partners. Our laboratories operate under CLIA, CAP, NYS, and FDA frameworks — regulatory precision is built into everything we do.
Day-to-day responsibilities
Execute DNA extraction, PCR, and high-throughput sequencing protocols within a compliant QMS
Operate liquid-handling robotics and next-generation sequencers; perform routine maintenance and troubleshooting
Complete assigned runs—clinical specimens, reagent QC batches, validation studies, and special projects—accurately and on schedule
Log non-conformances, enter run data into the LIMS, and maintain documentation to Good Documentation Practice standards
Uphold GxP, GMP, GCP, and GLP requirements; fulfill high-complexity testing personnel obligations under 42 CFR 493.1495
Maintain continuing education credits required by applicable regulatory bodies
Handle human biological specimens and biohazardous materials according to established safety protocols
Seniority levels
(Level I)
Performs protocols with some supervisory guidance; escalates issues to lead or supervisor
Resolves routine and occasional novel process variations using up-to-date information
Communicates clearly during shift handoffs; keeps detailed records
May provide informal guidance to newer colleagues
(Level II)
Works with minimal direction; exercises considerable clinical initiative
Conducts training and competency evaluations for technician-level staff on high-complexity methods
Proposes procedural improvements to enhance team efficiency; understands when to upscale quality or timeline concerns
(Level III)
Operates independently; regularly applies educated discretion in decision-making
Drives process change recommendations backed by cross-functional knowledge
Proficient in laboratory automation and recognized for best-practice leadership
Qualifications
(Level I) — must meet one of the following
Bachelor's degree or higher in medical technology or laboratory science, or
Bachelor's degree or higher in a chemical or biological science
plus
at least 6 months of high-complexity molecular experience in a CLIA-certified laboratory
(Level II) — must meet all of the following
Bachelor's degree or higher in a relevant science or laboratory science field
Minimum 1 year of clinical lab experience in a high-complexity CLIA setting (or 2 years with a Master's degree or higher)
Minimum 3 years of hands-on molecular laboratory experience (or 2 years with a Master's or higher)
(Level III) — must meet all of the following
Bachelor's degree or higher in a relevant science or laboratory science field
Minimum 3 years of clinical lab experience in a high-complexity CLIA setting (or 2 years with a Master's degree or higher)
Minimum 5 years of molecular laboratory experience (or 3 years with a Master's or higher)
Demonstrated proficiency in laboratory automation and best practices
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