6 verification engineer jobs at 4 companies in Fort Wright, KY
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Senior Principal Mechanical Design Engineer
Mason, Ohio, United States
OnsiteFull Time
Stress Engineering Services: Provider of independent engineering design, analysis, and testing services.
15+ YOERequires an engineering bachelor's degree, PE license, 15+ years developing regulated medical devices, FDA product development and Design Controls expertise, team leadership, risk management, verification, validation, and client-facing consulting.
SolidWorks, Python, MATLAB, Minitab, JMP, ISO 14971, ISO 13485, IEC 60601, FDA, Design Controls, Design for Manufacturability (DFM), Design for Assembly (DFA), Product Lifecycle Management
EndoSec: Security software and cryptographic hardware for government and defense.
Experience in FPGA design, RTL/C/C++, Python, VHDL/Verilog, hardware security, system integration, and verification tools; must be able to obtain U.S. government security clearance.
BWI Group: Global manufacturer of automotive brake and suspension systems.
Design and implement embedded C/C++ software for vehicle control systems, perform testing and verification, support ISO 26262 and Automotive SPICE processes, and collaborate with cross-functional teams.
C, C++, MathWorks Matlab, Simulink, Stateflow, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft SharePoint, Cradle, Doors, Windchill, Vector CANalyzer, CANape, CANoe, dSPACE Toolset (TargetLink and ControlDesk), CAN, FlexRay, Ethernet, AUTOSAR
Midmark: Designs and manufactures medical, dental and animal health equipment.
4+ YOEBachelor's degree (or equivalent) and 4+ years relevant experience; deep embedded systems and firmware expertise, C/C++ proficiency, RTOS, debugging, technical leadership, and verification practices.
Jenkins, Travis CI, Git, Python, Jave, C, C++, Bluetooth Low Energy (BLE), CAN, JTAG/SWD, oscilloscopes, logic analyzers, packet sniffers
GenthermNASDAQ: THRM: Designs and manufactures automotive thermal and medical temperature systems.
3+ YOEBachelor's in biomedical engineering or related, 3+ years medical device engineering experience, design control and DHF, verification/validation, risk management (FMEA), ISO 14971/13485 compliance, EU MDR and regulatory/audit support.