• Facilitate Customer Quality relations, Customer Supplier Audits. Customer Non-Conformances and subsequent Corrective Actions, with full resolution by objective and meaningful evidence.• Maintained and improved the Quality Management System, procedures and production processes, with defect data trend analysis, root cause, failure resolution and corrective actions.• ISO 9001 Audit – Internal/External Audit and Certifications.• UL Listed Product Manager – Maintained UL audits, supported and updated procedures, test instructions. • Process Engineering Support.• Test Engineering Support.

Metabolic Test Systems• Facilitated Internal ISO 9001 Audits

● Facilitated Customer Quality relations, customer supplier audits. Customer Non-Conformances and subsequent Corrective Actions, with full resolution by objective and meaningful evidence.● Maintained and improved the quality management system, procedures and production processes, with defect data trend analysis, root cause, failure resolution and corrective actions.

● Facilitated Customer Quality relations, customer supplier audits and drove preferred supplier approval from those customers. Customer Non-Conformances and subsequent Corrective Actions, with full resolution by objective and meaningful evidence.● Maintained and improved the quality management system, procedures and production processes (SMT/Solder Reflow), with data collection for trend analysis, root cause, failure resolution and corrective actions. PFEMA based system. Facilitated process improved Tiger Team that increased First Pass Yield from 81% to 96%.● Facilitated the reduction of scrap by 30% by a process review team, implementing safe handling, processing and storage of product in process.● Site IPC J-STD-001 CIT - Certified Trainer, with prior IPC-A-610 Trainer certification.● Active FAA/EASA 145 Repair Station Chief Inspector and Repairman.● SAE Certified DQR Onsite Source Inspector for various major Aerospace Companies.● Certified AS9100 / ISO 13485 Internal Auditor - PEAR based audit system.● AS9100 / ISO 9001 / ISO 13485 Quality Systems Administration - Full AS9100 recertification audit, with no findings in 2021.● Facilitated onsite AS5553/AS6081 Counterfeit Mitigation and Detection protocol, system implementation and inspector training.● Monitored and reviewed supplier approvals, supplier audits, supplier quality ratings and administered supplier corrective actions.● Setup and performed Software Validation for ISO 13485 Medical Products Processing.● Experience with Conformal Coating systems and inspection, AOI Systems, X-Ray, ESS and Vibration Testing.

● Successfully maintained ISO 9001 compliance and registration while administering the Quality Management System. ● Developed and maintained quality system procedures and processes for trend analysis, root cause, failure resolution and corrective actions.● Managed customer relations, approvals, audits, quality ratings and corrective actions.● Managed and maintained Supplier approvals, audits, quality ratings and corrective actions.

● Successfully maintained ISO 9001 compliance and registration while administering the Quality Management System. Maintained, developed quality system procedures and processes for trend analysis, root cause, failure resolution and corrective actions.● Successfully managed Customer relations globally, including Quality Agreements and Plans, overall satisfaction and quality ratings.● Maintained Supplier approvals, audits, quality ratings and corrective actions.● Managed a full analytical test laboratory, developing properties procedures and processes.● Managed a team of quality inspectors and lab technicians.

● Successfully tasked with bringing the company into full ISO 9000 compliance and registration while administering the Quality Management System. This was accomplished by fully rewriting the quality system manual and quality procedures. Successfully performed all of the required internal and external ISO audits, as well as all internal and external Corrective and Preventive Actions for the Quality Management System.● A company consisting of 29 employees, and an average of $5 million annual sales, successfully managed the quality, engineering, design, and production of over 35 new Power Amplifier systems configurations and shipping of thousands of units.● Maintain a strong and diverse working knowledge of: o Quality Control and Quality Systems; o Electrical and Mechanical Engineering; o Printed Circuit Board (PCB) Design, Fabrication and Assembly; o Component Engineering; o Test Systems Functions; o Software and Firmware Development; o Configuration Management; and o Program Management.● Directly interfaced with Department of Defense (DOD) Prime Contractors, Sub-Contractors and Defense Contract Management Agency (DCMA) for contracts and quality source functions. Reviewed and administered COTS/MIL-SPEC Contracts, Statement of Works (SOW) and specifications for quality, engineering, production and cost proposals.● Successfully managed and mentored the team of engineers, technicians and assemblers that designed, fabricated and programmed a fully integrated National Instruments/LABView Power Amplifier Test System, producing an overall product test time reduction of 80%.● IPC-A-610 Certified Trainer.

● Managed and mentored the Quality Assurance and the Production Test departments.● Successfully developed and implemented methods, procedures, teams and processes to reduce defects - increase quality, streamline troubleshooting and increase Return On Investment (ROI).● ISO 9002 Coordinator, developing standards, certification programs and administering internal/external audits, compliance and certification processes, as well as external Corrective and Preventative Action processes.● IPC 610A Certified Trainer