Summary
Overview
Work History
Education
Skills
Timeline
Generic

Alexus Lyons

Tarboro

Summary

Detail-oriented and compliance-focused pharmaceutical professional with hands-on experience in GMP environments, specializing in batch record documentation and deviation investigations. Skilled in maintaining data integrity, collaborating with cross-functional teams, and ensuring regulatory compliance. Proven ability to support quality systems, drive process improvements, and contribute to inspection readiness efforts. Passionate about upholding quality standards and contributing to the safe production of pharmaceutical products.Experienced pharmaceutical professional with 6 years of industry experience, currently supporting manufacturing and deviation management at Thermo Fisher Scientific. Proven expertise in GMP-compliant production environments, with hands-on involvement in batch record documentation, deviation investigations, and CAPA support. Skilled at collaborating across departments—including QA, QC, and production—to ensure compliance, improve processes, and maintain audit readiness. Detail-oriented and process-driven, with a strong commitment to quality and regulatory standards in pharmaceutical manufacturing.

Overview

14
14
years of professional experience

Work History

Op 2

Thermofisher
09.2022 - Current
  • Worked successfully with diverse group of coworkers to accomplish goals and address issues related to our products and services.
  • Supported sterile fill-finish operations at a flagship pharmaceutical manufacturing facility.
  • Ensured ongoing compliance with GMP and FDA manufacturing standards.
  • Keep all rooms cleaned for manufacturing.
  • Support the Deviation Management Team by reviewing, investigating, and documenting GMP deviations in accordance with FDA and EU regulations.
  • Assist in identifying root causes of process and product deviations and collaborate with cross-functional teams to implement corrective and preventive actions (CAPAs).
  • Maintain and update records in the Quality Management System (QMS) (e.g., TrackWise, Veeva Vault).
  • Participate in Deviation Review Board meetings and help ensure timely closure of deviation records to maintain inspection readiness.
  • Perform data analysis to identify deviation trends and support continuous improvement initiatives.
  • Collaborate with QA, Manufacturing, Engineering, and Validation teams to ensure compliance with SOPs and regulatory expectations.

Filling Operator

Pfizer
08.2018 - 08.2022
  • Operated filling machines to ensure smooth production processes.
  • Monitored product quality during filling operations for compliance.
  • Maintained cleanliness and organization in the production area daily.
  • Conducted routine inspections of machinery to ensure optimal performance.
  • Followed safety protocols and guidelines during all filling operations.
  • Documented production data accurately for record-keeping purposes.
  • Calibrated measuring devices used for testing products before packaging.
  • Loaded and unloaded materials from pallets onto the production line.
  • Cleaned equipment as needed to maintain a safe working environment.
  • Inspected filled containers for accuracy and quality control.
  • Maintained accurate records of production, waste, and other related data.
  • Review and verify batch production records (BPRs) and batch packaging records (BPRs) for accuracy, completeness, and compliance with GMP and FDA regulations.
  • Identify and escalate discrepancies, deviations, or missing data within batch records to ensure timely resolution before batch release.
  • Collaborate with production, quality assurance (QA), and quality control (QC) teams to address documentation gaps and ensure batch documentation is inspection-ready.
  • Ensure real-time documentation during manufacturing processes to maintain data integrity and traceability.
  • Assist in batch record reconciliation and preparation for batch release by QA.
  • Maintain documentation logs and support archiving according to SOPs and regulatory guidelines.

Specialty Agent

Alorica
06.2017 - 07.2018
  • Managed customer inquiries and resolved issues through effective communication.
  • Utilized CRM systems to track interactions and maintain accurate customer records.
  • Collaborated with management to improve workflow processes and service delivery.
  • Conducted quality assurance reviews to ensure compliance with company standards.
  • Provided customer service to clients through phone and email communication.
  • Delivered excellent service via inbound and outbound calling efforts, meeting established minimum targets.
  • Responded promptly to customer service calls and inquiries from diverse groups of individuals.
  • Implemented marketing strategies to attract new clients.

Shift Manager

KFC
02.2011 - 05.2017
  • Supervised team members during busy shifts to ensure efficient service delivery.
  • Trained new employees on food safety and customer service protocols.
  • Managed inventory levels and ordered supplies to maintain stock availability.
  • Conducted regular quality checks to ensure food preparation met company standards.
  • Resolved customer complaints swiftly to enhance guest satisfaction and loyalty.
  • Scheduled staff shifts effectively to optimize coverage during peak hours.
  • Coordinated daily operations to maintain a clean and organized work environment.
  • Managed daily cash intake by counting out registers and tabulating profits.

Education

High School Diploma -

Tarboro High SChool
06-2013

Skills

  • Sterile processing

  • Quality control

  • GMP compliance

  • Production documentation

  • Fill-finish operations

  • Customer relationship management

Timeline

Op 2

Thermofisher
09.2022 - Current

Filling Operator

Pfizer
08.2018 - 08.2022

Specialty Agent

Alorica
06.2017 - 07.2018

Shift Manager

KFC
02.2011 - 05.2017

High School Diploma -

Tarboro High SChool

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Alexus Lyons