Summary
Overview
Work History
Education
Skills
Certification
Timeline
Generic

MINA SHENODA

Fort Worth,Texas

Summary

Reliable Medical Technologist I with excellent clinical laboratory skills. Successful at conducting and analyzing laboratory assays with high level of accuracy.

Overview

8
8
years of professional experience
1
1
Certification

Work History

Medical Laboratory Scientist-LC-CORE

Quest Diagnostics
Lewisville, TX
07.2023 - Current
  • Perform special chemistry analysis using hamlton, Liquid chromatograph mass spectrophotometry
  • Evaluated test results to determine if they are normal or abnormal; reported results to physicians in accordance with established protocols.
  • Maintained laboratory records and equipment; ensured compliance with safety regulations and quality control procedures.
  • Conducted research experiments related to clinical laboratory testing methods.such as validation of new reagent and quality controls
  • Prepared reagents and solutions used in laboratory tests according to standard recipes.
  • Investigated discrepancies between test results obtained by different technicians or laboratories.
  • Documented all findings accurately in electronic medical records system.
  • Calibrated instruments regularly according to manufacturer's specifications.
  • Performed maintenance tasks such as cleaning glassware and replenishing chemicals used during testing procedures.
  • Maintained clean and fully operational laboratory equipment.
  • Performed and documented preventive maintenance and quality control practices, noting best corrective action to remediate issues.
  • Maintained physical lab equipment, detecting malfunctions and troubleshooting to ensure optimum service.
  • Collaborated with laboratory staff to ascertain group needs and improve test accuracy.
  • Verified report accuracy by assessing statistics, specimen identification and critical values.
  • Promoted improved accuracy in laboratory testing review and reporting by leading efforts to present data.

Medical Technologist 1

Quest Diagnostics
Irving, TX
04.2022 - 07.2023
  • Conducted multiple tests at once using automated equipment (BECKMAN CULTER)and computerized instruments.
  • Reviewed test results to confirm accuracy and diagnosed causes behind irregular findings.
  • Planned and carried out regular maintenance on equipment by following procedures and manufacturers' guidelines.
  • Supported quality control processes by monitoring activities and reporting.
  • Documented medical test data and results in patient medical records.
  • Evaluated body fluids and tissue samples to document findings such as normal or abnormal results.
  • Conducted and evaluated quality control measurements to maintain equipment performance.
  • Evaluated and implemented new laboratory techniques and procedures using statistical methods and theoretical knowledge.
  • Prepared, stored and assessed liquid and solid reagents for precise and correct test results.

Lab Assistant

Quest Diagnostics
Irving, TX
08.2021 - 04.2022
  • work in extraction area in PDM department on Hamilton machines.
  • Maintained inventory and equipment and placed orders for laboratory supplies.
  • Handled administrative tasks for laboratory staff and overall operations.
  • Recorded known control values from technical instruments to boost reliability and accuracy in test results reporting.
  • Completed equipment maintenance and calibration tasks according to standards.
  • Expertly procured and processed specimens for laboratory staff.

Medical Laboratory Scientist

G-tech laboratories
Cairo, Egypt
02.2016 - 06.2018
  • Performed various tests on patients to assess needs and medication effectiveness.
  • Applied knowledge of microbiology, chemistry and hematology daily.
  • Reviewed patient data, prepared data reports and signed off on release of information requests.
  • Performed hematology analyses including complete blood count and differential, coagulation testing, and body fluid analysis.
  • Analyzed specimens for the presence of microorganisms using a variety of techniques such as culture, immunoassay, molecular diagnostics, and microscopic examination.
  • Evaluated test results to determine if they are normal or abnormal; reported results to physicians in accordance with established protocols.
  • Prepared reagents and solutions used in laboratory tests according to standard recipes.
  • Conducted research experiments related to clinical laboratory testing methods.
  • Monitored inventory levels of laboratory supplies; placed orders when necessary.
  • Documented all findings accurately in electronic medical records system.
  • Calibrated instruments regularly according to manufacturer's specifications.
  • Performed maintenance tasks such as cleaning glassware and replenishing chemicals used during testing procedures.
  • Collected specimen samples for clinical trials and assessment.

QA Specialist

Pharco Pharmaceuticals Factory
CAIRO, EGYPT
2014 - 2016
  • Performed manual and automated testing on web-based applications to ensure quality assurance.
  • Analyzed user requirements and created detailed test scenarios to validate the functionality of software products.
  • Identified, investigated and documented defects in the system.
  • Evaluated new features or enhancements from a quality assurance perspective.
  • Collaborated with developers in order to troubleshoot problems quickly and efficiently.
  • Executed end-to-end tests to ensure all components of the system are working as expected.
  • Verified accuracy of data entry into databases and ensured data integrity throughout the system.
  • Assisted in creating documentation related to QA processes such as Test Plans and Reports.
  • Monitored QA procedures for adherence by employees, notifying personnel of non-compliance issues.

Regulatory Affairs Specialist

Eva Pharma
CAIRO, EGYPTY
2012 - 2014
  • Maintained records of all regulatory filings and correspondence.
  • Collaborated closely with cross-functional teams on product design, manufacturing processes, quality assurance.
  • Reviewed and compiled regulatory documents to ensure compliance with international regulations.
  • Developed strategies to obtain FDA approval for new products.
  • Coordinated submission of product applications to various regulatory agencies.
  • Assisted in the preparation of technical documentation for registration submissions.
  • Monitored changes in legislation related to medical device regulation, labeling, and marketing claims.
  • Provided guidance on interpretation of applicable laws and regulations governing product development activities.
  • Managed communications with health authorities during the review process of new products.
  • Managed regulatory change required by new and revised laws and regulations, communicating complex requirements and identifying operational impacts.
  • Researched new regulatory requirements for registration requirements in different markets.

Regulatory Affairs Associate

Eva Pharma
CAIRO, EGYPT
2008 - 2012
  • Reviewed and evaluated regulatory documents to ensure compliance with applicable regulations.
  • Developed and maintained a database of regulatory information for assigned products.
  • Identified potential issues related to product registration and notified management accordingly.
  • Assisted in the preparation of responses to questions from global health authorities regarding regulatory matters.
  • Monitored regulatory activities within the industry and provided reports on findings.
  • Analyzed customer complaints related to product labeling and packaging issues and investigated root causes.
  • Assisted in preparing reports required by local health authorities regarding safety monitoring activities.
  • Provided technical review of data or reports to ensure scientific rigor, accuracy and clarity.
  • Evaluated changes to documents submitted to determine need for amendments.

Education

Bachelor of Science - Animal Science, Biology , Chemistry, Histology

Suez Canal University
Ismailia, Egypt
07.2007

Skills

  • Regulatory Compliance
  • Specimen Handling
  • Equipment Maintenance
  • Safety Guidelines
  • Report Preparation
  • Laboratory Management
  • Supply Management
  • Equipment Operation
  • Quality Control
  • Sample Testing
  • Data Analysis
  • Technical Troubleshooting
  • Safety Regulations
  • Testing Protocols

Certification

  • Certified Pharmacy Technician (CPhT)
  • CPR Certification
  • Immunization Certification

Timeline

Medical Laboratory Scientist-LC-CORE

Quest Diagnostics
07.2023 - Current

Medical Technologist 1

Quest Diagnostics
04.2022 - 07.2023

Lab Assistant

Quest Diagnostics
08.2021 - 04.2022

Medical Laboratory Scientist

G-tech laboratories
02.2016 - 06.2018

QA Specialist

Pharco Pharmaceuticals Factory
2014 - 2016

Regulatory Affairs Specialist

Eva Pharma
2012 - 2014

Regulatory Affairs Associate

Eva Pharma
2008 - 2012

Bachelor of Science - Animal Science, Biology , Chemistry, Histology

Suez Canal University

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MINA SHENODA