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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in architecting and implementing FPGA-based and embedded software systems for medical devices, ensuring compliance with regulatory standards and best practices. Proven ability to lead cross-functional teams and mentor engineers throughout the product development lifecycle.
Highest-signal resume keywords
FPGA DesignEmbedded Software DevelopmentC/C++ ProgrammingMedical Device ComplianceContinuous Integration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
FPGA DevelopmentVHDLVerilogSystemVerilogSoC FPGAEmbedded LinuxRTOS DevelopmentDigital Signal ProcessingRequirements TraceabilityRisk Management
Soft Skills
Technical LeadershipMentoringCollaboration
Tools & Technologies
AMD/Xilinx VivadoIntel QuartusGitAutomated BuildsCI/CD
Industry Keywords
IEC 62304ISO 14971ISO 13485Design History FileQuality Management System
Tech Stack
Tools & technologiesLinuxRTOSC++
About the role
Key responsibilities & impact- Architect, design, implement, integrate, and verify complex FPGA-based and embedded software systems for medical devices
- Drive hardware/software partitioning, system-level architecture, and technical tradeoff decisions
- Translate user and system needs into software, FPGA, and subsystem design requirements
- Establish FPGA development and verification best practices, coding standards, reusable test frameworks, self-checking testbenches, automated regression, coverage-driven verification, scripted workflows, automated builds, and Continuous Integration
- Lead FPGA design activities involving timing constraints, multiple clock domains, high-performance data paths, fixed-point arithmetic, real-time control, signal processing, and hardware/software interfaces
- Serve as technical authority across development programs and lead architecture and design reviews
- Resolve complex technical issues, explore emerging technologies, and develop reusable technology roadmaps
- Ensure compliance with medical-device design controls, software lifecycle processes, risk management, traceability, and applicable regulatory standards
- Support regulatory submissions, audits, and QMS deliverables
- Lead development and review of requirements, architecture, design, verification, risk management, and Design History File documentation
- Provide cross-functional technical leadership from concept through commercialization
- Mentor engineers and collaborate with Systems, Electrical, Quality, Regulatory, Clinical, Manufacturing, Product Management, and Project Management teams
Requirements
What you’ll need- Bachelor’s degree in Electrical Engineering, Computer Engineering, Software Engineering, or related engineering discipline
- 8+ years of relevant embedded software experience
- Experience developing embedded software and FPGA-based systems, including FPGA design, implementation, integration, and/or verification
- Experience with FPGA development languages and technologies, such as VHDL, Verilog, SystemVerilog, SoC FPGA, or comparable FPGA platforms
- Experience leading or contributing to complex embedded product development, including architecture, requirements, system integration, and verification
- Experience programming in C/C++
- Experience with FPGA development tools and platforms, including AMD/Xilinx Vivado and/or Intel Quartus
- Experience with embedded Linux and/or RTOS development, hardware/software co-design, and FPGA-based digital signal processing
- Knowledge of FPGA and embedded software verification, including simulation, static/dynamic analysis, coverage analysis, Git, automated builds, and CI/CD
- Experience with medical device or regulated product development, including requirements traceability, risk management, and standards such as IEC 62304, ISO 14971, and ISO 13485
Benefits
Comp & perks- Hybrid work flexibility
- 20% travel allowance/requirement
