Serve as manager for the service / install department.Serve as manager and lead for the robotics group.

Serve as one of six members on the management team responsible for the sustainability of Hill’s Supply as a company, as well as the development of several new processes. Serve as manager and lead for the robotics group.Lead or heavily support all aspects of robotics at Hill’s, including sales, marketing, procurement, billing, outside resource management, barn design, layout, installation, maintenance, and service. Act as technical lead for additional products beyond robotics, including advanced automation, refrigeration, and herd management software.Support all activities of the service department, including bidding, scheduling, installation, service, and maintenance. Work with both electrical and mechanical components, including low voltage, high voltage, networking, communication, control circuits, sensors, transformers, circuit boards, contactors, relays, timers, refrigeration, pneumatic power, hydraulic power, vacuum power, pumps, welding, and fabricating.

Served as technical lead and manager for the hardware team, managing the team on multiple development and sustaining projects while continuing to strive for their successful completion as established by their specification and schedule.Expanded the hardware team from one electrical engineer, two technicians and an intern to nine electrical engineers, four technicians and an intern. Worked closely with recruiters and human resources during this growth initiative. Managed several simultaneous projects, including multiple new generation designs, old generation re-designs and improvements, future product design experiments, and various other sustaining activities.Developed, maintained, communicated, and presented development schedules to other departments and collaborated with these departments as necessary to coordinate release schedules.Aided in the development and formation of the project management team.Conducted ongoing development schedule reviews to locate opportunities for accelerated development and efficiency improvements, including leveraging outside resources where appropriate to enhance development cycle timelines.Identified and coordinated several outside resources from individual component design to cradle-to-grave box build designs and production. Was responsible for department budget creation and tracking.Collaborated with other engineering managers to establish development standards and system-wide design standards across all development platforms.Served as lead interface for engineering during all ISO and FDA audits.Was responsible for the hardware design, certification, and regulatory approval for a new international market in Japan. Coordinated efforts (personnel and test equipment) and executed the majority of testing during expedited on-site UL safety testing. Completed expedited Japan Radio Act testing and approval by coordinating and acting as technical lead for both Japan and US-based certified body test labs.

Served as lead electrical engineer responsible for new LifeVest hardware designs as well as required sustaining efforts.Served as Scrum master for the hardware team during the agile Scrum development process.Served as team lead for company-wide strategic planning sessions.Was responsible for creation and sign-off of engineering design and development plan as required per ISO 13485.Helped complete the largest FDA submittal with the LifeVest product.Analyzed 2nd edition versus 3rd edition IEC 60601 requirements, completed gap analysis, and tested products for 3rd edition compliance.Served as key interface for engineering with manufacturing, customer support, quality, regulatory affairs, and materials.Served as lead interface for engineering during all ISO and FDA audits.Completed several design studies on future product functions, including size reduction techniques, pacing and pacing recovery improvements, dry ECG electrode improvements, and a new charger cost reduction design.Completed design, schematic capture, PCB layout, board-up, and verification testing of two projects, including a new cost reduction charger and new patient ECG interface design.Completed new generation animal and software verification testing during FDA submittal and received FDA approval in 2009.Identified root cause and design fixes for released systems as required, including PCB manufacturing issues, manufacturing component level issues, and design issues.Served as lead interface for engineering to FDA for several submittals, including design improvements, manufacturability improvements, and component level RoHS conversion.Redesigned required PCBs to improve manufacturability and remove modifications while supporting FDA submittal and approval.

Served as one of two electrical engineers responsible for the new generation wearable cardiac defibrillator hardware design, test, release to manufacturing, manufacturing test, and sustaining support.Completed design requirements and test protocols while holding required reviews per ISO 13485 requirements.Completed hardware design for all electrical hardware that is included within the wearable defibrillator. Solely completed schematic capture, component selection, and PCB layout for eight board designs, the most complex being eight layers with 5/5mil width and spacing. Design includes low level analog, high speed digital, power, and high voltage. Completed hardware board-up and debug of all eight board designs. Completed board, sub-assembly, and final assembly level hardware verification testing.Completed IEC 60601 safety testing, including extensive IEC 60601-1-2 EMC, EMI, and ESD testing.Worked closely with contract manufacturers on board level design for manufacturability and long lead time component issues.Worked with and coordinated multiple consultants for support, including component level reliability analysis, regulatory safety requirements definition and test protocol, and high speed digital timing and signal integrity analysis.Designed and tested hardware for manufacturing's board and system level automated test fixture "AutoTest.”Aided in compiling the new generation FDA submittal in 2008, which received FDA approval in 2009.Supported previously released systems by testing and debugging EMI issues, performing timing analysis and re-layout for memory obsolescence, debugging and fixing flyback converter noise immunity issues, as well as other various component availability and reliability issues.

Installed electrical devices in commercial, industrial, and residential areas.Performed work per customer specifications while adhering to NEC requirements.