• Performing sample prep, DNA extraction and PCR.
  

• Running KingFisher Flex, Accufill, VeritiPro, QuantStudio 12K and 5.
  

• Performing accurate manual and electronic pipetting of small sample volumes.
  

• Adhere to laboratory’s quality control policies, quality control activities and SOP’s.
  

• Review all SOP’s and workflow updates in a timely manner and ensure all SOP updates are implemented in real time for workflow processes.
  

• Perform preventive maintenance checks and decontamination of equipment and workspaces.
  

• Follow the laboratory’s established polices, and procedures for notifying appropriate supervisors when test systems are not within the laboratory’s established acceptable levels of performance.
  

• Facilitate and ensure appropriate individual work output is completed based on current company metrics.
  

• Identify problems that may adversely affect testing performance or reporting of test results by immediately notifying the General Supervisor and/or Technical Supervisor.
  

• Participate in processing proficiency testing samples, as applicable.
  

• Successfully complete all CEU credits as required by the company.
  

• Responsible for staying informed of all incident reports and compliance related issues by attending all team meetings.
  

• Ability to perform basic accession in pre-analytical operations: requirements for Patient Identifiers (PID), auditing and communicating client manifest issues, identifying specimens categorized as non-compliant, acceptance/rejection of patient specimens, and creating cases for exceptions and sent out orders.
  

• 60 semester hours or equivalent from an accredited institution that, at a minimum, includes either 24 semester hours of medical laboratory technology courses, OR 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology, and 12 semester hours of chemistry, biology, or medical laboratory technology in any combination.
  

• Completion of a clinical laboratory training program approved or accredited by the ABHES, NAACLS, or other organization approved by HHS (note that this training may be include in the 60 semester hours above).
  

Requirements: 

• 1-year high complexity clinical laboratory experience preferred, unless required by the state in which the laboratory is located.
  

• Broad understanding of sterile technique, contamination control, and unidirectional workflow necessary for a PCR lab.
  

• Prior knowledge of molecular laboratory techniques and processes, including but not limited to micropipette.
  

• Experience working in a CLIA/CAP laboratory is required.
  

• Basic understanding of instrument maintenance and troubleshooting.
  

Certifications/Licenses

•  ASCP, AMT, or other organizations preferred unless required by the state in which the laboratory is located.
  

f you, or someone you know, would like to be considered for this position, please apply today to discuss the next steps!