Omarr France
Arlington
Summary
Methodical Quality Inspector known for high productivity and efficient task completion. Possess specialized skills in defect identification, compliance monitoring, and process improvement. Excel at critical thinking, problem-solving, and communication, ensuring top performance in maintaining quality standards.
Methodical professional in quality control and assurance field, known for being highly productive and efficiently completing tasks. Possess specialized skills in precision measurement, defect identification, and regulatory compliance which ensure adherence to industry standards. Excel in problem-solving, communication, and time management, making significant contributions to team success and product excellence.
Seasoned Quality Inspector with background in verifying products meet specified standards and regulations. Strong expertise in conducting inspections, identifying defects, ensuring compliance to quality standards, and documenting inspection results. Known for strong analytical skills, ability to interpret blueprints and technical documents, and commitment to continuous improvement. Previous roles resulted in improved product quality, streamlined processes, and enhanced operational efficiency.
Results-driven Quality Control Inspector touting many years of experience examining manufactured products to detect deviations and defects. Dynamic collaborator well-versed in reading and interpreting blueprints and specifications and monitoring overall operations. Familiar with quality testing machines and methods.
Overview
21
21
years of professional experience
1
1
Certification
Work History
Senior Quality Inspector
Verify
Irving
05.2021 - Current
- Company Overview: Aerospace/Defense/ FAIR Inspection
- Performs First Article Inspection (process/reviewing) in according with Aerospace Standard AS9102
- Reviewing FAIR packages in house and ensuring the accuracy and completeness of all engineering design requirement records towards AS9102 conditions
- Confirms all aspect of the First Article Inspection Record (FAIR) is accurate and completed for a part number or assembly and that all parts, products, and characteristic accountability dimensions prior to approval
- Expertise in evaluating Purchasing documentation, specifications, shop planning, drawing, 3D modeling and various technical instructions
- Interpretation of engineering drawings, CMM data, digital product definition interpretation
- Responsible for Customer Relations, conflict resolution, as well as, all aspects of AS9102 training towards customer resolutions
- Aerospace/Defense/ FAIR Inspection
Quality Associate/Interim Quality Assurance Manager/Warehouse Operations
Monarch PCM
01.2016 - 01.2018
- Responsible for a wide range of comprehensive projects, operations, warehousing, purchasing, and quality initiatives
- Including all aspects of Quality Assurance Management, in conjunction with all developmental protocols, procedures, as well as, new product development, customer complaints, deviations, and internal audits
- Evaluate and approve all documents according to organizational and FDA regulation requirements, as well as, maintaining knowledge on all awareness issues and recommended strategies
- Performance quality audits on various systems for internal customers, preparing quality reports concerning all regulatory issues in all aspects of the manufacturing and packaging areas, responding with recommended solutions towards quality compliance
- Evaluated and prepared Standard Operating Procedures, measuring all aspects toward fulfilment of quality systems
- Conducted and maintained all aspects of quality system towards the creation, fulfillment, tracking, and/or elevation of deviations, NCP's, ECR's, ECN's and/or Corrective Actions and Preventive Actions initiatives
- Maintain and update all production records and evaluate all procedures, monitoring all new regulations of organization
Medical Device Robotic Manufacturing Quality Analyst/Quality Control Operations
Medivative Technologies
01.2014 - 01.2016
- Responsible for the performance of Quality Assurance/Engineering/Quality Control activities related to Incoming inspection, component manufacturing and final product assembly for the organization including device history record review and approval, ensuring linkage between nonconformance reports and actions to be completed before final product release
- Provide Quality Assurance/Quality System expertise regarding product quality principles are applied/Quality Systems Regulations and Medivative standards are met
- Participate a member of cross functional teams, as assigned to ensure quality principles and meditative standards are achieved
- Provides direct QA oversight for all activities during component manufacturing and final product assembly
- Serve as auditor for review, authorization, and disposition of device history records (DHRs)
- Perform incoming inspection activities for drug products, product labeling, device parts, and assemblies according to approved inspection procedures
- Perform device constituent testing for release of production lots and stability testing
- Perform Document Control activities related to the management of Quality Systems documentation and records
- Develop and maintain QA/QC procedures
- Management of electronic records for produce builds
- Utilize system and knowledge of pending nonconformance and change control activities to determine if all appropriate corrective and/or preventive actions have been completed prior to release of product
- Initiate non-conformance reports as required
- Perform quality/product investigations as assigned including determination of root cause and propose disposition of non-conforming materials
- Develop proposals for related corrective and preventive actions
- Performing C.A.P.A processes in conjunction with NCR regulatory priorities
- Review product, process and engineering change requests, validation and non-standard processes as assigned
Quality Assurance Lab Technician
The Coca Cola Company
01.2014 - 01.2015
- Responsible for conducting qualitative and quantitative testing of raw materials and finished goods
- Conduct qualitative and quantitative microbial testing of beverages, syrups, and raw materials and equipment throughout the entire production process
- Analyze syrup beverage and water attributes
- Audit container rinsers, air blowers, filters, and coders to ensure proper operations
- Conduct package quality inspection and quality audits and isolate product that does not meet standards
- Receive and test CO2 and all raw materials prior to production process
- Maintain highest possible housekeeping standards to prevent microbial contamination
Bio Chemical Operator II
Eli Lilly
01.2011 - 01.2014
- Initiated, developed, and processed various portions of the cultured media implementation for the creation and production of Bio-Human Synthetic Human Insulin
- Identified improvement cost savings of 8.7million dollars by redirecting and utilizing current vessel attributes
- Utilized both computer based, as well as, manual process to help manipulate the culture base through differing computer and technological methods: Delta V, S.A.P, Compliance Suite-DCS Interface, Pegasus, PI Data Historian, Measurex, HPLC Analyzers, and Lab Support
- Implementation and induction of culture media through various stages of the fermentation processes
- Monitored, updated, and utilized Standard Operating Procedure
- Executed Batch Production Records and procedural instructions
- Collected and recorded using data to monitor and control processes
- Promoted quality initiatives in relation to Current Good Manufacturing Practices (cGMP) guidelines
- Reviewed and identified abnormal processing conditions and escalated to appropriate engineering personnel
- Promoted safety and environmental compliance in all designated areas assigned by departmental manager, as well as, in conjunction within designated area as Environmental Committee Member
- Provided corrective actions necessary for improvements to batch records, procedures, and automation to technical services and engineering
Supervisor
Roche Diagnostics
01.2004 - 01.2008
- Supervised a team of 50-75 manufacturing and production staff
- Recognized for leading team with integrity and new ideas in improving process flow for consistently while exceeding expectations in all areas including quality audits, curing aged inventory accounts
- Requested for participation and involvement in special project management team assignments based on proven ability to excel with minimal supervision
- Maintained and enhanced training procedures for all team members for safety, quality and production policies and procedures
- Interpreted specifications and job orders to production team
- Developed, recommended and implemented measures to improve production methods, equipment, performance, and quality of product
- Created work Standard Operating Procedures (S.O.P) with various departmental management to ensure and exceed customer projected deadlines
- Analyzed and resolved production issues utilizing Corrective and Preventive Action (CAPA) systems
- Inspected and measured parts and products to verify conformance to specifications
- Reduced defective outflow production orders in process defects and scraps to minimize departmental losses
Aerospace Tooling Inspector Calibration Inspector Optics Inspector
PPG Aerospace
- Responsible for the analysis and overall operational processes for final and intermediate verification of any and all materials and products that are in process, as well as, leading the manufacturing facility
- Authorized to maintain and facilitate new calibration procedures, as well as, initiating new mechanisms to correlate company initiatives and new methodologies
- Creation, maintenance, and initiation of calibration and database operations for the documentation of all in-house calibration methods and procedures
- Contractor Liaison in response to all areas of calibration operations
- Incoming inspection processes for various materials for production
- Creation and review of First Article Inspections
- Manufacturing/Production dimensional checks for accuracies that meet all documented standards according to engineering manufacturing prints
- Assist with documentation and corrective actions
- Creation of Certificate of Conformance and supportive documentation for shipment preparation
- SME (Subject Matter Expert)
- Train-the-Trainer for various areas of production and quality initiatives
- DQR(Direct Quality Representative)
Education
MBA -
Interdenominational Theological Center
United States12.2024
Bachelors of Science - Total Quality Management
Indiana Institute of Technology
United States12.2024
Associates Degree - Business Finance
Indiana Institute of Technology
United States12.2024
Skills
- Manufacturing
- Corrective action
- Engineering
- Aerospace and Defense
- Calibration
- Optics
- Machine Tool
- Train-the-Trainer
- Standard Operating Procedures (SOP)
- Quality Assurance
- Internal Audit
- Product Development
- Purchasing/Procurement
- Warehousing
- Auditing
- Change Control
- Document Control
- Drug Products
- Quality Control
- Testing
- Beverages
- Housekeeping/Cleaning
- Automation
- Current Good Manufacturing Practice (cGMP)
- Cost Control
- Environmental Compliance
- GMP (Good Manufacturing Practices)
- High Performance Liquid Chromatography (HPLC)
- Corrective and Preventative Action (CAPA) Systems
- Process Flow
- Project/Program Management
- Finance
- Conflict Resolution
- Continuous Improvement
- Customer Relations
- Engineering Drawing
- Hazardous Materials/Substances
- Inventory Management
- Leadership
- Preventative Maintenance
- Security Clearance
- Six Sigma
- Team Building
- Top Secret Clearance
- Total Quality Management (TQM)
- Operations Processes
- Operational Audit
- Documentation
- Support Documentation
- Quality Management
- Operations Management
- FDA Requirements
- Problem Solving Skills
- Reporting Skills
- Regulatory Reports
- Monitor Regulations
- Medical Equipment
- Manufacturing Analysis
- Regulations
- Cross-Functional
- Quality Engineering
- Systems Administration/Management
- Document Management
- Records Management
- Proposal Development
- Accounts Payable
- Root Cause Analysis
- Process Engineering
- Engineering Change Order
- Engineering Change Management
- Product Reviews
- Laboratory
- Analysis Skills
- Materials Testing
- Blowers
- Insulin
- Distributed Control Systems (DCS)
- Fermentation
- Safety Compliance
- Process Improvement
- Team Lead/Manager
- Manufacturing Management
- Safety/Work Safety
- Time Management
- Standards Development
- Six Sigma Certification
- ISO (International Organization for Standardization)
- Quality System Requirements (QSR)
- C Programming Language
- Vendor/Supplier Relations
- Lean Manufacturing
- Technical/Engineering Design
- Application Servers
- Requirements Management
- 3D Modeling
- Procurement Specifications
- Educational Technology
- Capability Maturity Model (CMM)
- Customer Training
- Quality assurance
- Process improvement
- Supplier evaluation
- Project management
- Problem solving
- First-article inspection
- Effective communication
- Surface inspection
- Presentation skills
- SAP software
- Production streamlining
- Cross-functional collaboration
- Precision measurement
- Inspection procedures
- Visual inspections
- Quality control
- Materials knowledge
- Measurement techniques
- Multitasking capacity
- Equipment calibration
- Materials testing
- Calibration equipment validation
- Continuous improvement
- Professional demeanor
- Inspections and reviews
- Reliability
- Time management
- Communication skills
- Non-conformance reporting
- Multitasking
- SOLIDWORKS and MATLAB
- Training and mentorship
- Product tests
- Problem-solving
- Calibration techniques
- Professionalism
- Production monitoring
- Operations monitoring
- Quality processes
- Equipment operation
- Goal setting
- Packaging and shipping support
- Specifications reading
- Teamwork and collaboration
- Task prioritization
- Analytical thinking
- Dependable and responsible
- Conflict resolution
- Excellent communication
- Critical thinking
- [Equipment] operation
Certification
- Training the Trainer
- Leadership and Exploration Preparedness Training
- Subject Matter Expert (S.M.E)
- Master Scheduling
- Management Liaison for Safety Committee Operations
- Powered Industrial Vehicles (PIV)
- QSR's
- GMP
- ISO
- Six Sigma Certification (pending)
- DQR
- Certified in AS9102 Rev B / AS9102 Rev C
- Government Clearance
- Secret Security Clearance
- DQR Designated Quality Representative
Awards
- Supervised a team of 50-75 manufacturing and production staff.
- Recognized for leading team with integrity and new ideas.
Languages
English, Intermediate
Timeline
Senior Quality Inspector
Verify
05.2021 - Current
Quality Associate/Interim Quality Assurance Manager/Warehouse Operations
Monarch PCM
01.2016 - 01.2018
Medical Device Robotic Manufacturing Quality Analyst/Quality Control Operations
Medivative Technologies
01.2014 - 01.2016
Quality Assurance Lab Technician
The Coca Cola Company
01.2014 - 01.2015
Bio Chemical Operator II
Eli Lilly
01.2011 - 01.2014
Supervisor
Roche Diagnostics
01.2004 - 01.2008
Aerospace Tooling Inspector Calibration Inspector Optics Inspector
PPG Aerospace
MBA -
Interdenominational Theological Center
Bachelors of Science - Total Quality Management
Indiana Institute of Technology
Associates Degree - Business Finance
Indiana Institute of Technology
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