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4 дня назад

Quality Control Technologist I-III (AI)

23 - 28$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior/middle/senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Quality Control Technologist I-III (AI): Supporting quality control in a high-volume genomics laboratory by maintaining equipment and reagent compliance across clinical, R&D, and modeling workflows with an accent on QC evaluations, equipment maintenance, and regulated documentation. Focus on analyzing QC data, investigating laboratory issues, implementing corrective actions, and maintaining CLIA/CAP/NYS-DOH/ISO compliance.

Location: Chicago, Illinois, United States. Full-time, onsite laboratory role. Sunday–Thursday, 8:00 a.m.–4:30 p.m.

Salary: $23.25–$28.50 per hour in Illinois.

Company

hirify.global develops a proprietary precision-medicine platform that connects real-world evidence with clinical insights to support treatment decisions.

What you will do

  • Support quality control activities in a high-volume molecular and genomics laboratory.
  • Create and implement equipment functionality and reagent processes for R&D, clinical, and modeling laboratory staff.
  • Schedule and track performance qualifications, preventive maintenance, equipment relocation, repairs, and routine maintenance.
  • Prepare reagents and execute and document quality control evaluations for new reagent lots.
  • Collect and analyze QC data, monitor performance metrics, investigate deviations, and support corrective and preventive actions.
  • Maintain SOPs, equipment records, maintenance logs, QC documentation, and audit materials while training staff and troubleshooting laboratory issues.

Requirements

  • BS in medical technology, clinical laboratory science, chemistry, physics, biology, or a related science.
  • Ability to analyze QC data and monitor assay or instrument performance metrics.
  • Strong problem-solving, communication, organization, documentation, and time-management skills.
  • Experience maintaining records and documentation in a controlled system.
  • Moderate experience with Microsoft Excel or Google Sheets.
  • Able to occasionally lift up to 40 pounds.

Nice to have

  • At least one year of experience in a molecular laboratory or with laboratory liquid handlers.
  • Experience in a clinical laboratory regulated by CAP, CLIA, NYS-DOH, or ISO.

Culture & Benefits

  • Work in a cutting-edge genomics workflow supporting precision medicine.
  • Participate in laboratory audits with QA, pharmaceutical, and regulatory bodies.
  • Benefits may include incentive compensation, restricted stock units, medical coverage, and other benefits depending on the position.
  • Maintain a clean, organized, and compliant laboratory environment.

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