Molecular Technologist I

1 month ago


Alpharetta, United States Fulgent Genetics Full time
About Us

Fulgent Genetics is a leading cancer testing and diagnostics laboratory with a strong reputation for helping pathologists and oncologists diagnose and treat cancer patients.

Our company has a rich history, dating back to 2011, and has evolved into a premier full-service genomic testing company built around a foundational technology platform.

We offer a wide range of testing services in oncology, anatomic pathology, infectious and rare diseases, and reproductive health.

Our goal is to redefine the way medicine is managed for patients and clinicians alike by providing effective, flexible testing options and best-in-class service and support.

Job Summary

Under general supervision, the Molecular Technologist I will be responsible for performing and reporting high-throughput, clinical genotyping assays using molecular platforms, operating and maintaining laboratory equipment, and increasing productivity and maintaining proficiency in the wet lab and analysis sections.

Key Responsibilities
  • Extract and quantify DNA and RNA from blood and tissue samples.
  • Perform PCR reactions.
  • Perform specified assays for genotyping services in accordance with the SOP.
  • Prepare and evaluate test results for completeness, accuracy, and quality.
  • Report test results in LIS.
  • Receive, unpack, and log customer samples according to SOPs.
  • Perform troubleshooting, maintenance, and calibration of instrumentation and equipment used to conduct testing in compliance with quality control/assessment standards.
  • Participate in the development and/or maintenance of SOPs as required.
  • Identify ways to improve laboratory procedures and activities.
  • Optimize diagnostic tests and update existing standard operating protocols.
  • Work with laboratory supervisor for troubleshooting and determining solutions.
  • Participate in lab meetings and generate ideas for improving efficiency and productivity.
  • Comply with all aspects of laboratory safety, safety stations, safety manuals, safety SOP, and MSDS sheets.
Qualifications

The ideal candidate will have a BS in biological science or equivalent with at least one year of training/experience, MB (ASCP) Certification, and lab experience and/or training in a clinical laboratory setting.

Preferred experience in molecular pathology and superior communication, time management, and organizational skills are also required.

The candidate must satisfy requirements for high complexity testing under CLIA regulations and be able to work in a fast-paced environment with exposure to biological hazards associated with human specimens.



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