To obtain a position where I can use my knowledge and experience to make a positive impact on a company.
Experienced with quality management processes and methodologies. Utilizes comprehensive quality control techniques to enhance product standards and ensure compliance. Strong understanding of team leadership and continuous improvement strategies.
Overview
16
16
years of professional experience
1
1
Certification
Work History
Administrative Assistant
Jewel Case Corp
01.2025 - Current
Handling the incoming phone calls for the entire office on a multiline phone system.
Maintaining documentation within the office including inventory, invoices, accounts receivable, order confirmations, and packing slips.
Handling correspondence for the CEO, Operations Manager, and Customer Service Manager.
Supporting staff is all aspects of the day to day business.
Managing and maintaining office, warehouse, and janitorial supplies.
Working collaboratively with all departments to ensure cross functional success.
Supplier Quality Manager
HPNE
01.2023 - 10.2024
Review supplier quality data to identify process improvement opportunities.
Work closely with suppliers to improve product quality, delivery times, and resolve issues.
Conduct thorough supplier audits, ensuring strict compliance with quality standards.
Managed complex quality issues, driving significant improvements in supplier performance and product reliability.
Pioneered advanced quality systems through strategic database management and in-depth analysis. Revamped documentation processes, enhancing internal audit efficiency and inspection accuracy.
Spearheaded comprehensive training programs on quality-related areas, including 5S and Lean methodologies. Fostered a culture of continuous improvement across the organization.
Served as primary liaison with external customers on quality matters, effectively resolving concerns and strengthening relationships. Maintained robust calibration systems for optimal performance.
Analyzed supplier quality data, identifying process improvement opportunities. Conducted audits to ensure compliance with quality standards.
Quality Control/Quality Assurance Manager
G-Form, LLC
05.2022 - 11.2022
Product Specification & First Article approvals
New Item documentation
Keep company audit ready at all times.
Manage CAPA for internal deviations
Manage CAR/SCAR
Ensuring proper GMP Documentation
Conduct Internal audits annually, across all departments.
Conduct Management reviews.
Responsible for site safety
Ensure product quality consistency.
Manage two employees.
Check new tooling created on-site.
Verify mold and die accuracy.
Supervise SEI Testing and Sample sizes.
Check outgoing shipments for accuracy.
Work with the production manager for training
Implement new strategies to improve yield.
Quality Assurance and Social Compliance Manager
Fit & Fresh, Inc
05.2021 - 05.2022
Control the Supply Chain in China, Korea, and Cambodia
Ensure product specifications are accurate and up to date.
Manage testing with 3rd party testing labs in the US and China
Manage Retail driven testing programs.
Review CAPA’s submitted by suppliers.
Investigate consumer complaints received via web and Customer Service
Implement Standard Operating Procedures as it relates to quality.
Coordinate audits per retailer requirements
Review and Approve label claims.
Manage the Quality Budget
Quality Manager
Diversified Distribution
02.2018 - 05.2021
Product Specification approvals
Address deviations from Customers regarding Private Label product
New Item documentation
Keep company audit ready at all times.
Manage and host all 3rd party audits.
CAPA responses from Social and GMP audits
Manage CAR/SCAR
Scheduling of audits for UL, Intertek and BV as needed.
Status meetings with customers
Ensuring proper GMP Documentation
Conduct annual GMP training for the site.
Conduct Internal audits annually, across all departments.
Conduct Management reviews.
Responsible for site safety
Ensure product quality consistency.
Manager two team members
Client Manager
Intertek Testing Services
12.2013 - 02.2018
Provide regular weekly updates with CVS team (or as appropriate) to discuss project goals, deliverables, status, etc
Act as single point of contact between CVS and Intertek
Schedule and Release program audits for Regulated and non-Regulated sites
Track all audit activity
Update and maintain SKU database including Vendor, Manufacturing Site, Packaging site, and Country of Origin
Approve and manage CAPA submissions for supply chain
Follow up with delinquent CAPA submissions.
Trouble shoot issues escalated by the scheduling teams
Maintain database with accurate contact information for entire supply chain
Resolve scheduling conflicts for supply sites
Control the full CVS Schedule of over 1,000 annual audits
Maintain accurate category management for all CVS supply sites
Triage potential new item alerts for manufacturing, packaging, holding, and subcontractor information. Approve items in a timely manner
Global Complaints & Consumer Affairs Coordinator
Kaz Incorporated
09.2009 - 11.2013
Expertise of the Consumer Calls process and the Oracle application
Good Understanding of Medical Device and Consumer Device Complaints, Reporting Requirements, Corrective and Preventative Actions and Complaint Investigations
Excellent Understanding of Consumer Affairs workflow and activities.
Review all consumer calls on a daily basis and evaluate them for reporting, investigations, Corrective action and any Field actions
Follow through with investigators to complete Complaint Investigations and ensure that they are completed in a timely manner
Follow through with Complaint reporting in a timely manner so that they are completed in a timely manner within the reporting requirement timeframe
Complete Medical Device Reporting and CPSC related reporting documentation
Follow thru with CAPA investigators to ensure that they are completed in a timely manner
Communicate with foreign offices and supplies to ensure timely and accurate information for DHR and Complaint Closure.
Test and Verify all Regulatory software testing.
Maintain and own the Complaint System
Participate in Usability Studies for new products as both moderator and observer
Responsible for EPA and FDA Establishment Registration as well as State Registration for Pesticides, 25(b) and FIFRA Exempt products.