Dre'Shawn Goode-Legette
Mebane,NC
Summary
Knowledgeable and self-motivated Associate Scientist with 5+ years of experience in qPCR, quality control and proper laboratory techniques. Possesses a B.S. in Biology and expertise in Microsoft Office and laboratory information management systems (Labware LIMS). Eager learner who rapidly grasps new ideas and integrates them into desired results.
Overview
4
4
years of professional experience
1
1
Certification
Work History
Associate Scientist QC-ARD
Pfizer
Durham, NC
12.2022 - 02.2024
- Perform release, stability and in process stat testing for analytical method transfer/qualification/validation for biological therapeutics
- Conduct all work according to appropriate Standard Operating Procedures' following Good Manufacturing Practices/Good Laboratory Practices (GMP/GLP) requirements and ensure integrity of all data generated and documented
- Perform data entry duties associated with pharmaceutical and biological GMP data
- Independently analyze and provide conclusions regarding experimental data generated
- Organize data received from multiple sources and enter the data into a validated database.
Data Entry Specialist
Eurofins
Durham, NC
03.2022 - 12.2022
- Perform data entry duties associated with pharmaceutical and biological GMP data
- Organize data received from multiple sources and enter the data into a validated database
- Archive the data received and maintain Excel spreadsheets as needed.
Research Associate
RHO
Durham, NC
09.2021 - 03.2022
- Writing external correspondence to internal and external stakeholders including emails, memos, minutes, and reports
- Formatting documents and creating document templates through Microsoft word
- Creating and formatting Case Report Forms, manual of operations documents, and other study-related documentation
- Maintain company website with communication.
Technologist
LabCorp
Research Triangle Park, NC
07.2020 - 06.2021
- Follows the laboratory’s procedure for specimen handling and processing, test analyses, reporting and maintaining records of patient test results
- Performs proficiency testing and documentation for all tests performed in accordance with CLIA, state and accreditation standards
- Adheres to the laboratory’s quality control policies; documents all quality control activities, instrument and procedural calibrations and maintenance performed
- Identifies problems that may adversely affect test performance or reporting of test results and corrects the problem or immediately notifies the Laboratory/Technical Supervisor, Laboratory Manager and/or Technical Director.
Education
BS in biology with a Concentration in Ecology and Evolutionary Biology -
Western Carolina University
05.2020
Skills
- Stability/release testing (qPCR, ELISA, pH, UV Vis, Appearance)
- Technical Writing
- Quality Control
- Labware LIMS
- Problem Analysis / Resolution
- Data Verification
- Data Entry
- Sample Handling
- Team Oriented
- Multitasking
- SQL
- Microsoft Excel
- Data Accuracy
- Assay Qualification
- Electronic Lab Notebook Documentation
- Safety Processes and Procedures
- Standard Operating Procedure Development
- GxP Compliance
- Results Analysis
- Data Analytics
- Molecular Biology
Activities
- Pfizer Global Black Community College Resource Group
- Pfizer DCMF Safety Team
Certification
Coursea Foundations: Data, Data, Everywhere Feb 23, 20204
Timeline
Associate Scientist QC-ARD
Pfizer
12.2022 - 02.2024
Data Entry Specialist
Eurofins
03.2022 - 12.2022
Research Associate
RHO
09.2021 - 03.2022
Technologist
LabCorp
07.2020 - 06.2021
BS in biology with a Concentration in Ecology and Evolutionary Biology -
Western Carolina University