John D'Arcy work email
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John D'Arcy personal email
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I am a veteran Systems and Software Verification Engineer with 15 years' experience in test planning, development, execution and analysis in the Biotech and Medical Device fields. My work includes system and software verification, data acquisition and analysis, and scripting for data analysis.
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Product Verification EngineerVarianSanta Clara, Ca, Us -
Product Verification EngineerVarian Nov 2021 - PresentPalo Alto, Ca, Us -
Software Verifcation EngineerJohnson & Johnson Medical Devices Companies Jun 2021 - Nov 2021New Brunswick, New Jersey, UsJohnson & Johnson Medtech. Santa Clara, CA.Verification of software components for a Linux-based, surgical robotics system in adherence with FDA regulation in an Agile testing cycle.Duties include but not limited to:● Performed verification of software for subsystem and component operations.● Performed verification of hardware motion in response to software commands.● Performed verification of software subsystems including GUI, logging, controls.● Executed bug verification tests in simulated and full system environments.● Identified and reported software and system bugs.● Identified testing weaknesses and commented on tests per run. Provided practical solutions for updating tests to meet all objectives. -
Software Verifcation EngineerAbbott Oct 2020 - Jun 2021Abbott Park, Illinois, UsAbbott Diagnostics Division. Santa Clara, CA.Verification of software components for a hematology system in adherence with FDA regulation in an Agile testing cycle.Duties include but not limited to:● Identified testing weaknesses and filed related bugs. Provided practical solutions for updating tests to meet all objectives.● Performed ad hoc and formal verification of software for general sample processing, additional assay-specific features.● Performed subsystem logging, system service, daily and weekly maintenance verification.● Performed verification of hardware motion in response to software commands.● Performed test execution review. -
Software Quality EngineerVarian Medical Systems Mar 2019 - May 2020Palo Alto, Ca, UsVerification of software and risk mitigation components for radiotherapy system in kV and MV energy ranges in the Agile development methodology.Duties include but not limited to:•Wrote test cases for test case automation.•Wrote test automation scripts in Python for testing of software •Test automation of software features included GUI features, login, system operations. •Identified defective requirements in tests for hardware caution labeling and related service manuals•Drove change in defective requirements and rewrote related tests•Performed verification of software for patient treatment, system service, daily maintenance.•Performed verification of hardware motion in response to software commands.•Performed verification of risk mitigation measures. -
Sr. Software Integration And Test EngineerIllumina Jun 2018 - Nov 2018San Diego, Ca, Us•Responsible for API integration over HTTPS•Reported software bugs and functional issues to 3rd-party software vendor. Worked with vendor to resolve issues.•Supported in-house software engineers to integrate product server software with vendor software.•Supported system engineering group to integrate software with sample preparation system. •Performed requirements review for data-conversion software from test perspective. -
Software Verification EngineerGeneweave Dec 2015 - Jan 2018GeneWEAVE Biosciences, A Division of Roche Molecular Solutions, Los Gatos, CA.Software Verification of a new luciferase-based medical device for screening of potential bacterial infections in adherence with FDA regulation and ISO standards. Waterfall development cycle.Duties included but not limited to•Primary responsibility for User Interface test development relative to software requirement specifications. Authored all UI test documents for early clinical and engineering releases of software. •Lead UI test development for final clinical software release.•Rewrote existing UI test documents to account for changes in UI requirements, appearance and function for final clinical release.•Responsible for language translation test development. Performed ad hoc testing in 5 languages. Outlined test procedure for upcoming launch version of UI software. Designed procedure to be interchangeable between languages. •Lead clinical database project from concept to testing in 12 weeks. Defined software requirement specifications, performed test planning, identified test protocol scope, authored test protocols, performed ad hoc, debugged, oversaw testing. Clinical database software met all requirements.•Performed test debug and execution for instrument software on embedded system.
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Systems EngineerRoche Molecular Systems Apr 2013 - Dec 2015Switzerland 🇨🇭 , ChRoche Molecular Diagnostics, Pleasanton, CA.System Development of a PCR-based medical device for blood screening in adherence with FDA regulation) and ISO standards in a BSL2 lab. Waterfall development cycle.Duties included but not limited to•Responsible for redevelopment of liquid classes critical to high-throughput customers; developed test protocols and execute verification; authored parameter and summary documents. 4 months time from investigation of liquid class settings to new settings in use on customer systems.•Responsible for personnel and laboratory resource management including system time, consumables and media to deliver redeveloped liquid classes. Supervised 2 system engineers and ran 3 systems for maximum efficiency late in development and during test execution phase.•Ensured product quality through analysis of data and investigation of anomalies. •Authored, debugged and rewrote test protocols for system-level verification.•Executed test protocols for user interfaces of all subsystems: sample pooling, sample processing, data management.•Performed ad hoc testing, bug reporting and bug fix testing from first beta to release candidate for multiple aspects of the system including UI.System Development of a PCR-based medical device for cancer diagnostics and characterization in adherence with FDA regulation and ISO standards in a BSL2 lab.Duties included but not limited to•Performed ad hoc testing to characterize behavior at system and component level during beta and release candidate development.•Performed ad hoc testing to investigate unexpected software issues during beta and release candidate development.•Developed and maintained ad hoc databases and import / export procedures to minimize time required to re-image and re-install during beta and release candidate development. Reduced time required to create a database from 4 hours to 20 minutes. -
Systems Integration EngineerAbbott Hematology Aug 2012 - Feb 2013Systems Integration and Test of a flow cytometry-based medical device for blood cell counts in adherence with FDA regulations and ISO standards during the design feasibility, development and integration phases.Duties included but not limited to•Developed subsystem integration test procedures and executed on prototype systems.•Performed troubleshooting on subsystem integration issues involving software, firmware and subsystem hardware.•Performed subsystem firmware and hardware operations using Python script language.•Wrote Python scripts for operation of and acquisition of data from subsystem hardware including valves, capacitive and electrical sensors, motors, LEDs and photodiodes.
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Systems EngineerRoche Molecular Systems Mar 2010 - Sep 2012Switzerland 🇨🇭 , ChSystems Development of a PCR-based medical device for blood screening in adherence with FDA regulations and ISO standards during the feasibility and development phases in a BSL2 lab. Waterfall development cycle.Duties included but not limited to•Performed Inaccuracy and Imprecision analysis on sample pooling process.•Authored, debugged and rewrote test protocols for pooling subsystem and database management software.•Performed ad hoc of system and all subsystems.•Evaluated system performance relative to established product requirements through system-level verification.•Evaluated subsystem performance relative to established product requirements through unit-level verification.•Analyzed quantitative data using JMP to verify operation of fluidics subsystem within tolerance. -
Systems EngineerLife Technologies Aug 2008 - May 2009Waltham, Ma, UsDevelopment of manufacturing tests for fluidics and thermal subsystems of genome sequencing system. Duties included but not limited to•Analyzed data using Minitab to develop test procedure and tools to test fluidics subsystem. •Drove assembly process changes to reduce leaks in fluidics system during test development.•Developed and documented test process to verify proper operation of thermal subsystem during manufacture.•Provided troubleshooting support to manufacturing group. -
Sr. Engineering TechnicianLife Technologies Oct 2007 - Aug 2008Waltham, Ma, UsProduction of genome sequencing system composed of Windows-Linux hybrid networked computing nodes and software-controlled peripheral hardware clusters. System integrates optics, 2-D electro-mechanical system for optical positioning, fluidics, thermal control and robotics.Duties included but not limited to•Performed top-down hardware troubleshooting to board level. •Assembled subsystems from individual components. Tested the completed subsystem.•Assembled system from subsystem level.•Performed quality control, calibration and testing of complete system.•Recommended design changes to optics and fluidics systems to improve technician and field service access to system. -
Scientist / Systems EngineerRapiscan Systems Mar 2004 - Sep 2007Experimental setup, prototype and pre-production testing, troubleshooting, data analysis, and failure analysis on complex electronic components and subsystems on multi-tiered LAN-based, Linux-native systems designed for Homeland Security threat detection.Duties included but not limited to•Performed subsystem- and system-level performance and failure/stress testing during system qualification.•Collected and analyzed data for patterns unique to satisfactory performance or failure; produce statistical analysis of data.•Developed and executed experiments to acquire data for algorithm development and to improve system performance.•Wrote in custom, in-house script language to calibrate and analyze data.•Performed data optimization to improve and/or replace previous formulations of simulated threats. •Performed troubleshooting of hardware and software on all systems from research to fielded level.•Tested and validated diagnostic and end-user software.•Established, documented and performed subsystem assembly processes.•Integrated system control, data acquisition systems and related electrical systems on research level systems.
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Administrative Support/Data EntryHumane Society Silicon Valley Oct 2003 - Jan 2004Temporary employment after relocation back to the Bay Area while seeking scientific employment.
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Physics Graduate Teaching AssistantGeorgia Institute Of Technology Aug 2002 - May 2003Atlanta, Georgia , UsTwo sections of physics labs per semester. Instruct students in lab procedures, experimental methods, and provide tutorial instruction on physical concepts. Graduate student in laser ultra-fast optics (including laser technologies).
John D'Arcy Skills
John D'Arcy Education Details
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California State University - East BayPhysics
Frequently Asked Questions about John D'Arcy
What company does John D'Arcy work for?
John D'Arcy works for Varian
What is John D'Arcy's role at the current company?
John D'Arcy's current role is Product Verification Engineer.
What is John D'Arcy's email address?
John D'Arcy's email address is jo****@****her.com
What schools did John D'Arcy attend?
John D'Arcy attended California State University - East Bay.
What skills is John D'Arcy known for?
John D'Arcy has skills like Root Cause Analysis, Quality Control, Test Development, Validation, Calibration, Troubleshooting, Fda, R&d, Design Of Experiments, Medical Devices, Software Documentation, Testing.
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