Mariah Taylor
***************@*****.***
Greenville, NC
Professional Summary
Results-driven Quality Assurance professional with over 5 years of progressive experience in pharmaceutical manufacturing, packaging, and quality operations at Thermo Fisher Scientific. Skilled in cGMP compliance, batch record review, in-process inspections, and documentation accuracy. Proven ability to identify and resolve quality issues, support CAPA investigations, and collaborate cross-functionally to improve process efficiency and product reliability. Strong background in operating within regulated environments using QMS, LIMS, and SAP systems. Committed to maintaining the highest standards of safety, quality, and continuous improvement in all aspects of production and compliance.
Core Skills
cGMP & FDA Compliance Quality Assurance & Control Batch Record Review & Documentation CAPA & Deviation Investigations In-Process Inspections & Testing Good Documentation Practices (GDP) QMS, LIMS & SAP Systems
Pharmaceutical Manufacturing Operations Packaging & Labeling Procedures Root Cause Analysis & Continuous Improvement Equipment Setup, Cleaning & Calibration Cross-Functional Team Collaboration Internal Audit Support
Data Integrity & Traceability Safety & Regulatory Compliance Professional Experience
Senior QA Technician, Thermofisher Scientific
Greenville, NC
July 2022 – Present
Perform in-process and final inspections to ensure products meet cGMP, FDA, and company quality standards.
Review batch records and documentation for accuracy, compliance, and data integrity. Support deviation and OOS investigations, assisting with root cause analysis and CAPA actions. Conduct sampling and testing of raw materials and finished products per approved SOPs. Maintain quality records and reports in QMS, LIMS, and SAP systems. Collaborate with cross-functional teams to resolve quality issues and drive continuous improvement. Assist with internal audits, training, and compliance readiness activities. Packaging / Labeling Technician II, Thermofisher Scientific Greenville, NC
July 2021 – July 2022
Operated and monitored packaging and labeling equipment to ensure products meet quality, safety, and regulatory standards.
Performed visual inspections of packaging components, labels, and finished goods to verify accuracy and compliance with cGMP and FDA requirements. Set up, cleaned, and maintained production lines according to established SOPs and batch records. Accurately completed documentation, including batch records, line clearance forms, and production logs, ensuring data integrity and traceability. Coordinated with Quality Assurance to resolve labeling or packaging discrepancies and implement corrective actions.
Handled materials in compliance with Good Documentation Practices (GDP) and company safety procedures. Supported process improvements and efficiency initiatives to optimize packaging throughput and reduce waste. Collaborated with cross-functional teams, including Production and Quality Control, to ensure timely order completion and compliance readiness.
Operator I, Thermofisher Scientific
Greenville, NC
Jan 2020 – July 2021
Operated and monitored pharmaceutical manufacturing and packaging equipment in compliance with cGMP, FDA, and safety regulations.
Set up, cleaned, and maintained production machinery to ensure efficient and accurate operation per SOPs and batch records.
Performed in-process inspections, measurements, and documentation to verify product quality and compliance. Accurately completed production logs, batch documentation, and equipment records following Good Documentation Practices (GDP).
Collaborated with Quality Assurance and Maintenance teams to identify and resolve equipment or process issues.
Followed safety procedures and maintain a clean, organized work environment to meet regulatory and company standards.
Supported continuous improvement initiatives to enhance efficiency, reduce downtime, and maintain product quality.
Education
High School Diploma JH Rose High School, Greenville, NC Technical Proficiencies
Systems & Software: SAP, LIMS, QMS, TrackWise, Microsoft Office Suite (Word, Excel, Outlook) Quality & Compliance Tools: cGMP, GDP, FDA 21 CFR Part 11, ISO Standards Testing & Inspection Equipment: Micrometers, Calipers, Scales, and Visual Inspection Tools Documentation & Reporting: Electronic Batch Records (EBR), Deviation Logs, CAPA Reports Manufacturing & Packaging Equipment: Blister packers, Labeling machines, Filling lines, Autoclaves, and Sterilization units
Process Support: Environmental Monitoring, Line Clearance, and Material Handling Ashley Martinez
********@*****.***
11/22/25
To Whom It May Concern,
I am pleased to write this letter of recommendation for Mariah Taylor, with whom I had the supervisor doing batch record review. During this time, Mariah consistently demonstrated exceptional professionalism, reliability, and a strong commitment to excellence in every aspect of her work.
Mariah is a quick learner who adapts seamlessly to new challenges and environments. She on projects that required both technical skill and critical thinking. Her initiative and problem-
Beyond her technical capabilities, Mariah is dependable and proactive. She can always be counted on to meet deadlines, maintain accuracy, and support her colleagues when needed. One of her standout qualities is her willingness to take on additional responsibilities—she frequently volunteered for new tasks and went above and beyond her role to ensure projects were completed to the highest standard. have no doubt she will continue to thrive and make valuable contributions wherever she goes. I wholeheartedly recommend her for any position she pursues. While I am no longer employed with ThermoFisher, please feel free to contact me at ********@*****.*** or 505-***-****
or performance in more detail.
Sincerely,
Ashley Martinez