Technical Supervisor Technologist
Resume:
Regina Lee
**** ******* *****, *****, ** *****
**********@*****.***
PROFESSIONAL SUMMARY
Lead Medical Laboratory Technologist with over two decades of experience in the field, office, and laboratory settings with a focus on
molecular nucleic acid testing to include HIV and various other infectious diseases. Highly organized and proficient in the organization
and execution of Immunology and Serology testing techniques. Seeking a career where I can add value to an organization by utilizing
my vast work experience and knowledge, education, and professionalism.
EMPLOYMENT HISTORY
Clinical Laboratory Scientist, Kelly Government Solutions, NIH. Bethesda, MD
June 2021-July2021
Accurately performs automated testing procedures for Serology based testing for infectious diseases using Ortho 3600
Performs DNA/RNA purification and quantitation, and real time PCR utilizing automated instrumentation such as
Amplipreptaqman; Cobas 6800
Organize daily workload based on priorities, rotation schedule and needs of the laboratory and patients
Independently analyzes and discusses the interpretation, reliability, and validity of test data
Accurately perform accessioning, specimen processing and test performance of moderate to high complexity tests
Communicate and consult with pertinent medical personnel regarding collection procedures, troubleshoot any problems
with specimen or documentation
Molecular Laboratory Technologist, Medix Scientific, Howard University Hospital. Washington, D.C.
August 2020-October 2020
Responsible for processing COVID-19 tests with results within 24 hours for staff and students.
Prepares samples for processing for RNA Isolation or RT-PCR processing using the COVID-19 TaqPath Combo kit.
Picks up samples from accessioning and sorts samples into appropriate racks.
Operation of computerized and automated instrumentation. quality control and maintenance, quality assurance, and test
results distribution.
Serology Team Lead Technologist, Henry M. Jackson Foundation for the Advancement of Military Medicine. Silver
Spring, MD
February 2019-June 2021
Serves as Team Lead for the Cap certified Clinical Serology laboratory to include the oversight of department staff and performance of
routine and specialized clinical assays and procedures by CAP approved clinical protocols in support of the HIV Diagnostics and
Reference Laboratory.
Reviews all clinical assay runs and maintenance logs to ensure adherence to standard operating procedures, conformance to
manufacturer’s specifications, and CAP standards.
Coordinates with Department staff to expedite workflow and maximize productivity to meet turnaround times and provide
recommendations for process improvements.
Verifies clinical patient results and performs final interpretation of complex algorithms for infectious disease testing.
Creates and updates standard operating procedures as needed
Involved in the interviewing, selection, evaluations, and corrective actions for staff members within the Serology Department.
Attends departmental meetings as required and works within cross-functional teams to identify and resolve complex laboratory issues.
Performs necessary supervisor functions in the absence of the Technical supervisor.
Medical Technologist, Henry M. Jackson Foundation for the Advancement of Military Medicine. Silver Spring, MD
August 2018 – February 2019
Performance of serological and immunological assays for the detection and confirmation of HIV (EIA, Western Blot, Geenius, and
Nucleic Acid testing) in a high throughput laboratory,
Perform specimen processing following laboratory SOP's, manufacturer guidelines, and CAP/FDA regulations.
Ensure compliance with all QA program requirements and document activities following established standards.
Ensure proper handling of specimens by assigned SOP's including but not limited to; proper data entry, storage, and aliquoting of the
specimens.
Perform and document all weekly, monthly, semi-annual, and annual maintenance and quality control procedures for instrumentation.
Responsible for developing, implementing, maintaining, and validating SOP's as required for the performance of clinical serological
testing.
Lead Medical Laboratory Technologist II, North Carolina Department of Health and Human Services. Raleigh, NC
May 2001 – July 2018
Lead Technologist for the acute HIV testing program, Rubella, and various Hepatitis viruses. Managed and trained employees; as well
as performed all HIV antibody negative serum specimens to ensure they were tested by an HIV-1 viral RNA NAAT (Nucleic Acid
Amplification Test).
Coordinated with department heads to identify was to maximize productivity to meet required deadlines, as well as provided
recommendations for workflow process improvement.
Attended departmental meetings as required and worked across various teams to identify and resolve intricate laboratory issues.
Performed necessary supervisor functions in the absence of the Technical Supervisor to include interviewing prospective new hires, as
well as provided feedback regarding peer performance within my department.
Maintained and trained new employees on the most recent procedures and instrumentation manuals, as well as the organization of all
methods verification studies as needed before the implementation of new equipment or assay procedure.
Managed the communications and relationships between the laboratory and its’ public health partners within the North Carolina
HIV/STD Prevention and Care Branch's STAT (Screening and Trace Active Transmission) Program and researchers at the University of
North Carolina. This included providing results and interpretations of a test as needed.
Conducted required tests utilizing various methods to include enzyme immunoassay (EIA), chemiluminescent immunoassay (CMIA),
and nucleic acid amplification tests (NAAT). Ensured all testing was carried out in compliance with federal statutes governing clinical
testing (CLIA) and employee safety (OSHA).
Created and disseminated detailed records of all acute HIV reactive cases, including follow-up specimens for confirmation of initial
patient results and specimens from the prospective partners. As the Lead Technologist, I was responsible for reviewing all reports before
release to ensure 1OO% accuracy in testing and reporting.
Developed, implemented, maintained, and validated standard operating procedures in conjunction with the Molecular Team and Quality
Assurance Group.
Coordinated and performed the validation of new assays, equipment, and materials as required.
Ensured the established Quality Control levels were upheld throughout the entire testing process from initial receipt of a specimen to
reporting of results.
EDUCATION
South Carolina State University
Orangeburg, South Carolina
Bachelor of Science, Biology
ASCP eligible
SKILLS
LIMS Proficient
CAP Proficient
Project Management Clinical Assays CLIA & OSHA Compliance SME
Quality Control Management SME
Medical Technology Methodology SME
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