Quality Assurance Warehouse Associate

Onyekachi Okoro, Ph.D., MBA

Phone:214-***-**** Email: ***********@*****.***

Address: **** ***** *****, **********, ** 75067

Summary of Qualifications

Versatile, results-driven, and dedicated professional, leveraging in-depth experience in driving quality standards and teaching/instructing others to improve academic and workplace performance. Solid organizational, communication, and time management skills. Adept at bridging learning performance gaps to complete operational interests, developing process improvement initiatives, and conveying complex teaching concepts simply and compellingly. Have worked with companies under FDA & FAA Regulations. Currently seeking Quality Specialist position in your organization, bringing 20+ years of related experience and key strengths as follows:

Quality Engineering Certified

Scrum Master Certified

Quality Assurance/Control

Internal Audit Support

Process Engineering

Billing & Collections

Technology Implementation

Statistical Process Control

Process Improvement

SOP Implementation

Research & Development

Regulatory Compliance

Team Collaboration

Staff Training/Teaching

Curriculum Development

Academic Standards

Course Coordination

Conflict Resolution

Delivering Instruction

Professional Experience

Goodier Cosmetics: Quality Control Incoming Inspector: June 2021-Present

In charge of incoming components

Using customer-provided Art Works to inspect and accept components

Segregating bad/contaminated components from good ones

Using SAP to release Accepted Components for production and hold Contaminated Components in the Hold Cage for Quality disposition

Helping QC Department in revising In-Coming Inspection Procedures

Perform Internal Audits

Preparing Non-Conforming Reports.

Soft Path LLC Staffing: Abbott Laboratories Quality Assurance Specialist II: Sept 2020 -May 2021

Worked on the production floor for the BinaxNOW COVID-19

Ensured that facilities and equipment used in the support of the Quality System are developed, validated, and maintained in compliance with regulatory and corporate requirements

Routinely performed final inspection of Device History Record (DHR)

Routinely created and maintained a Non-Conforming Material Report (NCMR) with Child Data and Quality Plans

Scraped Non-Conforming Material using ADMS and ADMS Mobile via PuTTY

Perform routine audits, collect rejected materials, and classify rejected materials into the right defect category

Provided daily updated reports to management and Improvement ideas if necessary

Graded Production labels with TruCheck software

CSRS Laboratories (Fort Worth, TX) Dynamic Medical Practice Feb. 2017 – May 2019

Responsible for managing the billing and collections process while reviewing patient documents and ensuring regulatory compliance of the clinic.

Consistently maintained the strictest confidentiality with patients.

Zodiac Aerospace (Gainesville, TX) Product Quality Auditor: Jan. 2014 – Mar. 2016

Squawked airplane seats per the company’s acceptance criteria

Used Engineering blueprints and specifications to monitor each stage of Plane Seat production

Conducted quality audits and surveys with Approved Work Orders

Audited products with engineering drawings and reviewed the production process.

Audited Incoming Products, Accepted Good Parts, and Rejected non-conforming Parts

Conducted analysis to address non-compliance issues, improving the quality of products.

Recommended changes and corrections of wrong procedures

Performed Final inspection of Airplane Seats per the regulatory requirements of the FAA

Tagged them with standards with the scope of the contract before shipping

KGBELLOS Residential Care, Inc. (Lewisville, TX) Administrator Jan. 2010 – Sept. 2013

Drove an increase in client referrals by analyzing to properly address patient issues.

Provided onsite training to CNAs, coordinated services, and collaborated with other departments.

Developed policies and guidelines for and obtained input from service personnel and provided professional input to related administrative systems.

Directed personnel rendering client care services and fostered public relations for the company.

Abbott Laboratories (Irving, TX) Quality Engineer Feb. 1985 – Oct. 2008

Held numerous positions in the Quality Management Organization in Abbott Laboratory Diagnostic Division a global leader in “in vitro” diagnostics.

Investigated DOA instrument failure caused by poor soldering on the Power Supply Board.

Served on the Material Review Board to evaluate non-conforming materials and make decisions to accept or reject, as well as wrote some operating procedures.

Ensured that all QA tests and issues were properly administered and investigated.

Generated DPUs (Defective Parts per Unit) Charts, Pareto analysis, and Quality cost reports.

Reduced shipping costs by developing audit-shipping lists to avoid shipping incomplete parts to customers.

Served in the company's internal audit team

Ensured that equipment used in the manufacture of products of the Quality System complies with regulatory and corporate requirements

Controlled Quality Documents, and Equipment Calibration and Validation Records

Participated actively in the process of ISO Certification of the company

Performed First Articles Inspection of products

Performed many vendor site audits before and after procurement agreements were signed

Education& Development

Certified Scrum Master – International Scrum Institute

Ph.D. in Applied Gerontology – University of North Texas

MBA in International Marketing – Texas A&M Laredo Campus

B.S. in Business Economics – Utah State University

Associates in Quality Technology – Tarrant County College

Certified Mediator – University of North Texas

Certified Quality Engineer – American Society for Quality

Certified Educator: Taught Economics, World Geography, and Statistics at High School

Started a program after school to help students

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