Cancer Genomics Technologist I - Certified

Fred Hutchinson Cancer CenterSeattle, WA
Onsite

About The Position

Under General supervision, perform cancer genomic laboratory procedures leading to the formation of accurate clinical reports using the International System for Cytogenomic Nomenclature. Works under the direction of the Technical Supervisor (or Section Director as defined in CAP.GEN.53400/CYG.50000) and technical guidance of senior techs with supervision from the lab operational leadership team. Uses discretion and judgment in carrying out procedures. This position will be full-time day shift, routine Sunday shift required; Sunday – Thursday schedule preferred.

Requirements

  • Bachelor's degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution or a Bachelor's degree and equivalent education and training as defined in 42CFR493.1489(b)(3)(ii). Must meet the CLIA education requirements for a high complexity testing
  • Typically, at least one year experience in a Cytogenetics/genomics lab OR completion of a formal certified training program in Cytogenetics/genomics
  • Certification as CG(ASCP)CM or MB(ASCP)CM or international equivalent with on-going documentation of CE comparable to ASCP programs
  • Basic knowledge of CAP guidelines
  • Basic knowledge of Cytogenetics or Cancer Genomics and related diagnostic testing
  • Basic Troubleshooting Skills
  • Good Attention to Detail
  • Solid Communication Skills
  • Solid Computer Skills
  • Sound Judgment
  • Work with limited supervision with routine tasks
  • Display personal responsibility and ownership for work
  • Demonstrate a mindset open to improvements and change
  • Must be able to differentiate between colors and pass a standardized color vision screen to perform this role

Responsibilities

  • Perform benchwork, analysis, and reporting of genetic or genomic assays consistently with a moderate level of accuracy and efficiency
  • Maintain lab areas and equipment including QC and validation documentation
  • Contribute to an environment of safety and focus on quality
  • Perform pre-director review of straightforward reports in areas of competency
  • Perform as assigned: Assist with the validation and implementation of new or improved processes
  • Assist members of lab management to improve operations, investigate and implement new technologies, streamline workflow strategies, organize, and evaluate QC/QM record
  • Assist with orientation and training of lab staff
  • Contribute to the continuing education of staff either through directly presenting material or investigating other resources

Benefits

  • medical/vision
  • dental
  • flexible spending accounts
  • life
  • disability
  • retirement
  • family life support
  • employee assistance program
  • onsite health clinic
  • tuition reimbursement
  • paid vacation (12-22 days per year)
  • paid sick leave (12-25 days per year)
  • paid holidays (13 days per year)
  • paid parental leave (up to 4 weeks)
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