2 days ago
Base Salary
$136k - $226k/yr
Responsibilities
- Lead architecture, design, implementation, integration, and verification of FPGA-based and embedded software systems for medical devices.
- Drive hardware/software partitioning, system architecture, technical tradeoffs, and translation of stakeholder needs into software, FPGA, and subsystem requirements.
- Establish FPGA coding, verification, testbench, regression, coverage, scripted workflow, automated build, and continuous integration practices.
- Lead complex FPGA design involving timing constraints, multiple clock domains, high-performance data paths, fixed-point arithmetic, real-time control, signal processing, and hardware/software interfaces.
- Provide technical leadership across programs, including architecture and design reviews, issue resolution, technology roadmaps, and engineer mentoring.
- Ensure compliance with medical-device design controls, software lifecycle processes, risk management, traceability, regulatory standards, audits, submissions, and quality-system deliverables.
- Lead requirements, architecture, design, verification, risk-management, and Design History File documentation while partnering with cross-functional teams.
Requirements
- Bachelor’s degree in Electrical Engineering, Computer Engineering, Software Engineering, or a related engineering discipline.
- 8+ years of relevant embedded software experience.
- Experience developing, implementing, integrating, and/or verifying embedded software and FPGA-based systems.
- Experience with FPGA development languages and technologies such as VHDL, Verilog, SystemVerilog, SoC FPGA, or comparable platforms.
- Experience programming in C/C++.
- Experience leading or contributing to complex embedded product development, including architecture, requirements, system integration, and verification.
- Master’s degree in a related engineering discipline is preferred.
- Experience with AMD/Xilinx Vivado and/or Intel Quartus is preferred.
- Experience with embedded Linux and/or RTOS development, hardware/software co-design, and FPGA-based digital signal processing is preferred.
- Knowledge of FPGA and embedded software verification, simulation, static/dynamic analysis, coverage analysis, Git, automated builds, and CI/CD is preferred.
- Medical-device or regulated-product development experience, including requirements traceability, risk management, IEC 62304, ISO 14971, and ISO 13485, is preferred.
Benefits
- Hybrid work arrangement.
- Annual travel requirement of 20%.
About Stryker
Stryker designs and manufactures medical devices and equipment for hospitals and surgeons, spanning orthopaedic implants, trauma and spine hardware, surgical tools, endoscopy, navigation, and patient care equipment. The NYSE-listed company, founded in 1941 and headquartered in Kalamazoo, Michigan, sells products and related services worldwide to health systems and ambulatory centers. It reported $22.6 billion in 2024 sales and markets its portfolio across roughly 75 countries.