Summary
Overview
Work History
Education
Skills
Accomplishments
Timeline
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Wa Shawnta Johnson

Cary,NC

Summary

Scientific professional skilled in histological techniques, contributing to accurate and timely diagnostic outcomes. Proficient in tissue processing, embedding, sectioning, and staining while maintaining high standards in laboratory environments. Emphasizes teamwork and adaptability for seamless operations and reliable support for pathologists and medical staff. Professional investigator with deep expertise in conducting thorough and precise investigations. Possesses strong analytical skills, critical thinking, and the ability to lead and collaborate effectively within a team. Known for adapting seamlessly to changing situations and consistently delivering impactful results. Highly skilled in evidence gathering, interviewing, and case analysis.

Overview

12
12
years of professional experience

Work History

Histotechnologist

The GI Guy
11.2024 - Current
  • Prepares histologic slides from tissue sections from microscopic examination and diagnosis by a Pathologist
  • Performs accessioning and grossing of specimens
  • Prepare sections of human tissue for examination
  • Operates computerized laboratory equipment to fix, dehydrate, and infiltrate with wax, tissue specimens to be preserved for study by a Pathologist within 48 hours
  • Stains and labels specimens
  • Performs special stains and immunohistochemistry procedures
  • Responsible for preventative maintenance and troubleshooting of equipment and laboratory computers
  • Keeps accurate records including but limited: equipment preventative maintenance and repair, QA and QC records, temperature and equipment charts, safety procedures, training, exposure and waste management
  • Prepares slides of specimens to enhance visibility under the microscope
  • Examines slides under the microscope to ensure tissue preparation meets laboratory requirements
  • Studies slides under the microscope to detect deviations from expected results and reports abnormalities for further study
  • Works within an approved budget; develops and implements cost saving measures; conserves organizational resources
  • Maintains Confidentiality of all patients
  • Adapts to changes in the work environment; manages competing and frequent demands, able to deal with frequent change, delays, or unexpected events

Lead Investigator, QC Compliance

Pfizer
07.2022 - 12.2024
  • Collaborated with cross-functional teams to achieve daily objectives
  • Conducted deviation investigations with strong communication and computer skills averaging 25 investigations to closure per month
  • Ensured site compliance with Regulations, ISO standards, corporate and company SOPs
  • Utilized SPS methodologies to drive sustainable process improvements
  • Facilitated training sessions on aseptic conduct and process enhancements

Aseptic Process and Compliance Process Area Specialist

Novo Nordisk
11.2020 - 07.2022
  • Led process improvement assessments for aseptic process batch deviations
  • Identified and evaluated safety gaps as the Work Wise Safety Representative
  • Collaborated assertively with stakeholders to prevent product quality deviations
  • Trained new hires in aseptic conduct and conducted cross-functional trainings
  • Ensured site compliance with Regulations, ISO standards, and SOPs

Chemistry Technician II

Novo Nordisk
05.2019 - 11.2020
  • Conducted chemical analyses to test character and nitrates
  • Collected and analyzed water samples in a cGMP environment
  • Trained team members with 4P certification
  • Collaborated with cross-functional teams to achieve daily goals
  • Performed Total Organic Carbon (TOC) and conductivity tests
  • Cleaned glassware and maintained laboratory cleanliness
  • Utilized gLIMS for data entry and reagent tracking
  • Handled minor deviations as needed and closed within 30 days
  • Maintained proficiency in testing and HPLC analysis appropriate
  • Analyzed raw materials accurately

Environmental Monitoring Technician

Novo Nordisk
03.2018 - 05.2019
  • Conducted environmental monitoring in a cGMP setting
  • Utilized PEMS software for monitoring purposes
  • Executed aseptic gowning certifications and environmental sampling
  • Trained new staff members when necessary
  • Collaborated with cross-functional teams to achieve daily objectives

Associate Quality Specialist

Merck
05.2016 - 12.2017
  • Conducted Critical Site Review for environmental monitoring test of two buildings
  • Trained and mentored new team members
  • Analyzed and interpreted environmental data for adverse trends
  • Participated in Kaizen events to improve processes
  • Authored Quality Notification investigations and assisted in product impact assessments

Bio-Processing Technician

Merck
10.2012 - 05.2016
  • Operated and monitored equipment in a cGMP environment
  • Performed routine sampling of Varicella using aseptic techniques
  • Calibrated, validated, and maintained equipment
  • Attended safety training and compliance events regularly
  • Investigated and reported questionable results
  • Executed environmental sampling of classified areas including active air sampling, surface sampling, and non-viabe air sampling
  • Provided summaries of test results to appropriate personnel as needed
  • Compiled and evaluated environmental data for adverse trends
  • Directly supported Performance Qualification and Requalification activities
  • Authored and assisted in Quality Notification investigations and product impact assessments
  • Collected and tested qualified Utility systems including Clean Steam, WFI and compressed gases

Education

Bachelor of Science - Biology

Martin University
Indianapolis, IN

Skills

  • Microsoft Suite
  • Leadership Skills
  • Time Management
  • Ability to Multitask
  • Communication Skills
  • Laboratory safety protocols
  • Teamwork orientation
  • Regulatory compliance awareness
  • Quality control adherence
  • Quality assurance adherence
  • CLIA guidelines
  • Quality control procedures

Accomplishments

  • Achieved Yellow Belt and Green Belt Certifications while working at multiple companies.
  • Selected to be a member of the Board of Directors for a nonprofit organization I served as a volunteer.
  • Achieved closure of an average of 25 investigations within 15-30 day deadlines by completing with accuracy and efficiency.
  • Achieve completing 100 - 200 special stains per week within 48 hours of collection dates.

Timeline

Histotechnologist

The GI Guy
11.2024 - Current

Lead Investigator, QC Compliance

Pfizer
07.2022 - 12.2024

Aseptic Process and Compliance Process Area Specialist

Novo Nordisk
11.2020 - 07.2022

Chemistry Technician II

Novo Nordisk
05.2019 - 11.2020

Environmental Monitoring Technician

Novo Nordisk
03.2018 - 05.2019

Associate Quality Specialist

Merck
05.2016 - 12.2017

Bio-Processing Technician

Merck
10.2012 - 05.2016

Bachelor of Science - Biology

Martin University
Wa Shawnta Johnson