Lead Molecular Technologist (3rd Shift)

Eurofins-posted 4 months ago
Full-time • Mid Level
Louisville, KY
Professional, Scientific, and Technical Services
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The Molecular Technologist Lead is responsible for specimen labeling, processing, test performance and storage, lab maintenance, supply stocking, logging temperature and lot numbers, aliquoting reagents, and following standard lab procedures, safety guidelines, and HIPAA policies. The position is also responsible for processing samples with molecular technologies other than TEM-PCR, such as qPCR. On days assigned as lead, also responsible for reviewing patient testing data and QC results, reporting test results, overall direction of patient testing, and communication of testing to Client Services, clients, sales, and the next lead. Responsible for training and competency assessment of testing personnel.

  • Follow standard operating procedure for specimen handling and processing, test analyses, and maintain accurate documentation for specimen traceability.
  • Adhere to established policies and procedures whenever test systems are not within acceptable performance levels.
  • Document all corrective actions taken when test systems deviate from established performance specifications.
  • Perform assigned TEM-PCR lab duties accurately and efficiently, including properly handling equipment.
  • Stock laboratory with supplies in addition to clean and decontaminate laboratory instruments and testing areas.
  • Setup and perform testing of samples for troubleshooting, clinical, and stability studies.
  • Setup and assist with validation and verification studies of laboratory tests.
  • Properly document records of studies performed, assuring traceability.
  • Perform assigned qPCR lab duties accurately and efficiently including properly handling qPCR equipment.
  • Adhere to all processes put into place by the Quality Assurance and Safety Officer.
  • Consult with the QC Supervisor and/or the Quality Assurance and Safety Officer about all quality concerns in a timely fashion.
  • Ensure reagents are QC tested before use with patient testing or concurrently with their first use.
  • Handle problems, troubleshooting, and judgment calls when situations arise that are not addressed in any procedure.
  • Review communication channels frequently to ensure all timely needs are handled and all updates are communicated properly.
  • Document processing errors, non-conformances, or deviations from standard procedure that may occur.
  • Coordinate any delayed testing and delay notifications according to policy.
  • Assure all repeat specimens and client error resolutions are in testing, and that no specimen is delayed testing due to an oversight.
  • Verify client errors and log them in the Laboratory Information System.
  • Direct the overall flow of testing, emphasizing efficiency, and TATs.
  • Enter, review, verify, and release patient results in the Laboratory Information System.
  • Ensure testing records are completed and filed appropriately.
  • Perform and document training and competency assessment for lab employees as assigned.
  • Maintain clear and accurate communication to Technical Supervisors and/or Administrative Operations Manager as needed.
  • Supervise daily performance of Molecular Technologist to ensure they are meeting our code of conduct and following all policy and procedures.
  • Provide documentation on all performance issues not covered in the nonconformance log.
  • Participate in the laboratory's quality assurance plan.
  • Participate in job specific training and annual competency assessment reviews.
  • Keep workstations clean according to the cleaning policy.
  • Wear personal protective equipment as required.
  • Observe all safety guidelines and report any unsafe conditions to a lab supervisor or manager.
  • Perform any additional duties as directed by Clinical Lab management.
  • Minimum of a Bachelor's of Science in Medical Technology, Clinical Laboratory Sciences, or a Life Science such as Biology or Chemistry.
  • Laboratory certification preferred.
  • Qualify as Testing Personnel as defined by CLIA rule § 493.1489.
  • Qualify as a General Supervisor as defined by CLIA rule § 493.1461.
  • Minimum 2 years' experience in a High Complexity Clinical Laboratory is preferred.
  • Must possess proficiency with basic computer programs.
  • Must be able to multitask and keep up in a fast-paced environment.
  • Must work well on your own with minimal supervision.
  • Must demonstrate key problem solving skills: active listening, analysis, research, creativity, communication, dependability, decision making, and team building.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.
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