(2006-2013) Responsible for daily activities of the Neonatal Transport Incubator production lines. Responsibilities include. Keeping production procedures and processes current and validated. Addressing quality issues, issuing nonconformance reports, disposition of nonconforming material.

Designed AC and DC distribution modules including terminal blocks relay logic and isolationIntegrated digital displays into the frame for monitoring onboard compressed gas pressure and consumption.Invented (see patent reference below) unique selector switch for displaying the pressure of the gas that is selected. Utilized Ratchet straps for securing gas cylinders into the frame assembly. Borrowed technology from snowboard bindings, implementation passed all vibration and crash… Show more Designed AC and DC distribution modules including terminal blocks relay logic and isolationIntegrated digital displays into the frame for monitoring onboard compressed gas pressure and consumption.Invented (see patent reference below) unique selector switch for displaying the pressure of the gas that is selected. Utilized Ratchet straps for securing gas cylinders into the frame assembly. Borrowed technology from snowboard bindings, implementation passed all vibration and crash testing to RCTA DO standards. Implemented T slot aluminum channels for mounting of auxiliary equipment.Designed the pneumatic circuit for Neonatal Ventilation and auxiliary gas delivery. Implemented cylinder mounted regulators with pressure transducers dropping pressure at the cylinder improving product safety. Implemented a venturi suction device saving space and weight in the overall design. Utilized Push to connect fittings in the pneumatic circuit improving production and service time. Achieved Electrical and Oxygen separation implemented a LED exam light in lieu of incandescent in the old design improving power consumption, and reducing weight. PATENTS FILED:Medical Air Compressor -PCT/US11/059180 filed November 3, 2011. US 13/697,215 filed November 9, 2012. Applications in China and EP as well, but have not received applications numbers yet.Electronic Valve Position Indicator - PCT/US11/051052 filed September 9, 2011Breathing Circuit Humidification System -PCT/US12/035644 filed April 27, 2012Transport Incubator -US 61/683,618 filed August 15, 2012 (provisional) PCT/US12/054287 filed September 7, 2012, US 13/713,955 filed December 13, 2012, US 13/714,072 filed December 13, 2012 (co -inventor)System and Method for charging a battery within a vehicle- Patent #8,384,344 -. Show less

(2008-2013)- Responsible for investigating all internal and external issues regarding the transport production line. Initiate Engineering Change Requests, with supporting documentation, Red lined Drawings, and suggested improvements.

Customer Complaint Investigations- responsible for review and approval of customer complaint responses generated by a Complaint Analyst. Determined Root Cause and Corrective Actions in order to prevent future occurrences. Direct interaction with customers to resolve issues. Disposition, review, and approval of internal and external Nonconformances. Revised and updated Martech Medical Products Validation program. Performed validations on various test methods. Reviewed and approved… Show more Customer Complaint Investigations- responsible for review and approval of customer complaint responses generated by a Complaint Analyst. Determined Root Cause and Corrective Actions in order to prevent future occurrences. Direct interaction with customers to resolve issues. Disposition, review, and approval of internal and external Nonconformances. Revised and updated Martech Medical Products Validation program. Performed validations on various test methods. Reviewed and approved validation protocols for Engineering, and Production. Initiation, Review, and Approval of Change Controls. Quality Audits- (Both Internal and External) responsible for demonstrating effectiveness of the Total Quality System, also responsible for initiating CAPA system for correcting audit findings. Customer Specification ReviewMade several Trips to a Martech facility in Mexicali, Mexico to provide validation training and guidance on several quality issues. Show less

Instrumental in obtaining and maintaining compliance to ISO13485:2003 certification. Managed the Quality Control testing laboratory, which includes 2 Supervisors and 30+ inspectors.

QA testing of Continuous Emissions Monitoring Systems (CEMS) and Data Acquisition & Handling Systems (DAHS) to meet customers EPA air quality permit requirements. Calibration and repair of Environmental Air Quality Gas Analyzers, including NO, NO2, CO, CO2, O2, NH3 and SO2 instruments. Responsible for Setup and testing of particulate monitoring opacity instruments.Plumbing of extractive flue gas sampling systems. Process improvements include designing new test fixtures and… Show more QA testing of Continuous Emissions Monitoring Systems (CEMS) and Data Acquisition & Handling Systems (DAHS) to meet customers EPA air quality permit requirements. Calibration and repair of Environmental Air Quality Gas Analyzers, including NO, NO2, CO, CO2, O2, NH3 and SO2 instruments. Responsible for Setup and testing of particulate monitoring opacity instruments.Plumbing of extractive flue gas sampling systems. Process improvements include designing new test fixtures and improving existing test procedures.Automation experience utilizing GE Fanuc, Allen-Bradley, and IDEC PLCs.Programmed two way serial communications between Gas analyzers and Programmable Logic Controllers.Familiar with Simplicity, ladder logic, and creating Graphical User Interfaces. Gas Chromatography Experience with TCD, FID, DID instruments Show less

· Design, and implement Validation Quality System. · Assist in the revamping of the Metrology program by defining Critical gauges vs. non-critical gauges.· Conduct validations of automated assembly equipment and laboratory test equipment.· Author and execution of Industry Standard IQ, OQ and PQ validation Protocols. Compliant to the Regulations of 21CFR 820 and 21CFR Part 11Define and document validation, and quality control protocols in compliance with GMP, FDA's QSR and… Show more · Design, and implement Validation Quality System. · Assist in the revamping of the Metrology program by defining Critical gauges vs. non-critical gauges.· Conduct validations of automated assembly equipment and laboratory test equipment.· Author and execution of Industry Standard IQ, OQ and PQ validation Protocols. Compliant to the Regulations of 21CFR 820 and 21CFR Part 11Define and document validation, and quality control protocols in compliance with GMP, FDA's QSR and ISO-9002 guidelines. Show less