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Staff Software Engineer- Medical Device Embedded SW (Hybrid)
full-timeGrand Rapids, Portage

Summary

Location

Grand Rapids, Portage

Type

full-time

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About this role

Work Flexibility: Hybrid or Onsite

We are seeking a highly experienced Staff Software Engineer to help design, develop, and maintain software for safety-critical medical devices. This role requires deep technical expertise in embedded and application software, strong technical leadership, and hands-on experience developing software in regulated medical device environments.

You will play a key role in defining software architecture, guiding technical decisions, and ensuring compliance with applicable FDA and international medical device regulations and standards, while remaining actively involved in development.

What You Will Do

  • Lead the design, implementation, and testing of medical device software in compliance with regulatory standards

  • Develop high-quality, maintainable software using C, C++, Linux, and Qt/QML

  • Ensure software development activities comply with IEC 62304 (Medical Device Software – Software Life Cycle Processes)

  • Participate in and support risk management activities in accordance with ISO 14971, including hazard analysis and risk controls related to software

  • Contribute to system-level requirements, software requirements, and traceability between requirements, design, implementation, and verification artifacts

  • Collaborate with Quality, Regulatory, Systems Engineering, and Hardware teams to support FDA design controls (21 CFR 820 / Quality System Regulation)

  • Support software verification and validation activities, including test planning, execution, and documentation

  • Participate in design reviews, code reviews, and technical risk assessments

  • Mentor engineers and establish best practices for compliant software development, documentation, and review processes

What You Need (Required Qualifications)

  • Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering or related disciplines

  • 4+ years of experience in software engineering, with experience with embedded systems

  • Extensive professional experience in software engineering with demonstrated staff-level technical leadership

  • Strong proficiency in C and C++ for embedded and system-level software

  • Hands-on experience with Qt and QML for application and user interface development

  • Experience working within a regulated development environment requiring formal documentation, reviews, and traceability

Preferred Qualifications

  • Experience with Real-Time Operating Systems (RTOS)

  • Knowledge of embedded and medical device communication protocols (e.g., UART, SPI, I²C, Ethernet, USB, CAN)

  • Experience implementing and maintaining CI/CD pipelines in regulated or embedded development environments

  • Experience with test automation, including unit, integration, and system testing

  • Familiarity with:

    • FDA Design Controls and submissions support (e.g., 510(k), PMA)

    • IEC 60601 considerations as they relate to software

    • Cybersecurity guidance for medical devices (e.g., FDA premarket cybersecurity guidance)

Travel Percentage: 20%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Other facts

Tech stack
Embedded Systems,C,C++,Linux,Qt,QML,Regulatory Compliance,Risk Management,Software Verification,Validation,Design Reviews,Code Reviews,Technical Leadership,Documentation,Test Automation,Real-Time Operating Systems,Medical Device Communication Protocols

About Stryker

Stryker is a global leader in medical technologies and, together with our customers, we are driven to make healthcare better. We offer innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. More information is available at stryker.com and careers.stryker.com.

Facts:
● 2024 Sales: $22.6 billion
● Industry: Medical Instruments & Supplies
● Employees: 53,000 worldwide
● 40 years of sales growth leading up to 2020
● 44+ Manufacturing and R&D Locations Worldwide
● $1.5 billion spent on research and development in 2024
● ~14,200 patents owned globally in 2024
● Products sold in ~75 countries
● Fortune 500 Company
● 7 consecutive years as one of Fortune's World's Best Workplaces

Stryker’s social media community guidelines: https://www.stryker.com/content/m/legal/social-media-community-guidelines/en/index.html

Notice Regarding Employee Conduct on Facebook/LinkedIn
Meta/LinkedIn does not permit employers to verify or validate “employees” in the (META: “Works at” LinkedIn: “Experience”) section of users’ profiles. Please be aware that the views expressed by individuals on their personal accounts and do not necessarily represent the views of our company. If you encounter any issues with a person claiming to be our employee, we recommend using the “Report Profile” feature. If you’d like to report concerns to our Ethics Hotline, you may do so at: https://app.convercent.com/en-us/LandingPage/b6bb4e84-9fcb-ea11-a974-000d3ab9f296

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Medical Equipment Manufacturing

What you'll do

  • Lead the design, implementation, and testing of software for medical devices while ensuring compliance with regulatory standards. Collaborate with various teams to support FDA design controls and participate in risk management activities.

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Frequently Asked Questions

What does a Staff Software Engineer- Medical Device Embedded SW (Hybrid) do at Stryker?

As a Staff Software Engineer- Medical Device Embedded SW (Hybrid) at Stryker, you will: lead the design, implementation, and testing of software for medical devices while ensuring compliance with regulatory standards. Collaborate with various teams to support FDA design controls and participate in risk management activities..

Why join Stryker as a Staff Software Engineer- Medical Device Embedded SW (Hybrid)?

Stryker is a leading Medical Equipment Manufacturing company.

Is the Staff Software Engineer- Medical Device Embedded SW (Hybrid) position at Stryker remote?

The Staff Software Engineer- Medical Device Embedded SW (Hybrid) position at Stryker is based in Grand Rapids, Michigan, United States and Portage, Michigan, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Staff Software Engineer- Medical Device Embedded SW (Hybrid) position at Stryker?

You can apply for the Staff Software Engineer- Medical Device Embedded SW (Hybrid) position at Stryker directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Stryker on their website.