Quality Control Medical Technologist

Regina Lee

Hampton, VA • 919-***-**** • **********@*****.*** • https://www.linkedin.com/in/regina-lee- b778a882

EDUCATION

South Carolina State University, Orangeburg, SC

Bachelor of Science - Biology ASCP Eligible

PROFESSIONAL SUMMARY

Resolute and highly skilled Medical Laboratory Specialist with over three decades of experience. Proficient in high-complexity testing using ELISA, PCR, and other immunological methods for clinical and research analysis. Organized and knowledgeable in Serology and Molecular Biology techniques. Seeking new challenges to positively impact laboratory operations or research success.

PROFESSIONAL EXPERIENCE

Riverside Peninsula Cancer Institute and Infusion Center – Newport News, VA 11/24 - Present

Medical Technologist

Perform technical laboratory procedures in Hematology, Chemistry, Serology, Blood Bank, Urinalysis, Microbiology, and Point of Care Testing.

Ensure accurate performance, review, and documentation of quality control and quality assurance guidelines.

Conduct routine maintenance, troubleshooting, and inventory control of laboratory equipment and instruments.

Participate in proficiency testing and maintain compliance with accreditation standards (CAP, DNV, AABB, CLIA, OSHA, etc.).

Accurately perform pre-analytical, analytical, and post-analytical testing for quality patient care.

Collaborate with physicians and multidisciplinary teams to communicate laboratory findings and support patient care.

Train and mentor new employees and students on laboratory procedures and protocols.

Maintain laboratory accreditation readiness, including validation testing, proficiency sample performance, quality control documentation, and temperature checks.

Adhere to hospital and departmental policies while upholding patient safety and national quality initiatives.

Perform specimen collection, processing, and phlebotomy as needed.

Unified Women’s Healthcare – Chesapeake, VA 05/24 - 10/24

Molecular Technologist

Perform molecular diagnostic testing for HPV, STIs, genetic screenings, and reproductive health conditions.

Conduct PCR, RT-PCR, nucleic acid extraction, and sequencing to analyze DNA/RNA samples.

Process and analyze gynecological specimens for infectious diseases and genetic markers.

Perform prenatal genetic testing for hereditary conditions and chromosomal abnormalities.

Ensure quality control, documentation, and compliance with CAP, CLIA, and FDA standards.

Maintain and troubleshoot molecular diagnostic instruments and laboratory equipment.

Collaborate with healthcare providers to communicate test results and support patient care.

Stay updated on advancements in molecular diagnostics and implement new testing methodologies.

Sinai Hospital - Baltimore, Maryland 08/22 - 04/24

Laboratory Supervisor

• Responsible for planning, coordinating, and directing daily activities in the central receiving section of the laboratory.

• Supervises and guides personnel, ensuring compliance with CAP, CLIA, and CLSI standards.

• Focuses on quality improvement and actively participates in the QA/QC program.

• Provides exemplary service to laboratory customers.

• Schedule management, resource allocation, and workflow coordination.

• Orienting and training section personnel.

• Developing and updating written section orientation for new employees.

• Implementing continuous quality improvement techniques.

• Enforcing health and safety regulations.

• Incorporating safety compliance into procedures.

• Performing benchwork during high workload or short staffing.

Meso-Scale Diagnostics LLC – Gaithersburg, Maryland

11/21 – 07/22

Bioanalytical Associate III

Managed biological samples, reagents, and materials to support sample testing and assay service projects.

Performed protein-based immunoassays on a routine basis with high throughput (2-8 plates per day).

Executed experiments and analyzed resulting data in support of reagent and assay development projects with minimal supervision.

Analyzed data using spreadsheets and graphing software.

Utilized BSL-2 techniques.

Initiated the verification of accuracy and validity of data, promptly correcting any errors.

Developed and implemented SOPs and participated in developing new documentation for the department.

Logged associated maintenance activities in accordance with documented requirements.

Maintained electronic inventory databases and records of processing, aliquoting, vialling, and labeling materials.

Kelly Government Solutions, National Institute of Health - Bethesda, Maryland

06/21 – 07/21

Clinical Laboratory Scientist

Accurately performed automated testing procedures for serology-based testing of infectious diseases using Bioplex assays.

Conducted DNA/RNA purification and quantitation, as well as real-time PCR, utilizing automated instrumentation such as Ampliprep TaqMan and Cobas 6800.

Organized daily workload based on priorities, rotation schedules, and the needs of the laboratory and patients.

Independently analyzed and discussed the interpretation, reliability, and validity of test data.

Accurately performed accessioning, specimen processing, and test performance for moderate to high complexity tests.

Communicated and consulted with pertinent medical personnel regarding collection procedures and troubleshooted any specimen or documentation issues.

Recorded, reported, and posted test results using LIMS software.

Executed corrective actions when test controls were outside specified limits.

Medix Scientific, Howard University Hospital - Washington, D.C. (Temporary)

Molecular Laboratory Technologist

08/21 – 11/21

Processed COVID-19 tests for staff and students, ensuring results within 24 hours.

Prepared samples for RNA isolation or RT-PCR processing using the COVID-19 TaqPath Combo kit.

Collected and sorted samples from accessioning into appropriate racks.

Prioritized work assignments and maintained accurate records.

Operated computerized and automated instrumentation, performed quality control, and oversaw maintenance.

Set quality assurance guidelines for laboratory work.

Verified specimen purity from saliva and nasal swab methods.

Henry M. Jackson Foundation (Military Medicine) - Silver Spring, Maryland

Serology Team Lead Technologist

08/18 – 06/21

Led the CAP-certified Clinical Serology laboratory, overseeing department staff and performing routine and specialized clinical assays and procedures according to CAP-approved clinical protocols in support of the HIV Diagnostics and Reference Laboratory.

Reviewed all clinical assay runs and maintenance logs to ensure adherence to standard operating

procedures, conformance to manufacturer’s specifications, and CAP standards.

Consistently adhered to Good Lab Practice (GLP) and safety protocols, producing accurate results compliant with regulatory standards.

Coordinated with department staff to expedite workflow, maximize productivity, and meet turnaround times, providing recommendations for process improvements.

Verified clinical patient results and performed final interpretation of complex algorithms for infectious disease testing.

Created and updated standard operating procedures as needed.

Participated in interviewing, selection, evaluations, and corrective actions for staff members within the Serology Department.

Attended departmental meetings and collaborated with cross-functional teams to identify and resolve complex laboratory issues.

Functioned as a supervisor by attending meetings, conference calls, and maintaining the lab in the absence of the Technical Supervisor.

Ensured laboratory compliance with all CAP/CLIA guidelines and laws.

Delivered superior training and leadership to teams, boosting performance, and helping team members achieve performance targets.

North Carolina Department of Health and Human Services - Raleigh, North Carolina

08/90– 07/18

Medical Laboratory Technologist I & II

Led the acute HIV testing program, Rubella, and various Hepatitis viruses.

Managed and trained employees, ensuring accurate testing using HIV-1 viral RNA NAAT and immunological assays.

Coordinated with department heads to optimize productivity and workflow processes.

Resolved intricate laboratory issues across teams.

Conducted supervisor functions, including interviewing new hires, and providing peer feedback.

Trained new employees in procedures and instrumentation.

Maintained relationships with public health partners and researchers.

Performed enzyme immunoassay (EIA), chemiluminescent immunoassay (CMIA), and nucleic acid amplification tests (NAAT).

Ensured compliance with CLIA and OSHA regulations.

Reviewed and released accurate acute HIV reactive cases.

Developed, validated, and maintained standard operating procedures.

Coordinated validation of new assays and equipment.

Upheld quality control levels throughout testing.

Participated in research projects.

Interpreted test results and troubleshooted assay problems.

SKILLS

ELISA and Bioplex assays

Western blotting

DNA & Protein Isolation

DNA Extraction

PCR

Liquid Handling Robotics

Nucleic Acid Purification

Fluor immunoassay

Exceptional Communication Skills

LIMS proficient

Writing SOP’s and Validations

Project Management Clinical Assays CLIA & OSHA Compliance SME

ASCP Eligible

Quality Control Management SME

Microsoft Excel, Word, and PowerPoint

BSL-2

Team Management

Strong Organizational and People skills

CLIA, CAP, FDA, and GMP

Contact this candidate