Responsibilities
- Conduct or design advanced prototyping, testing, research, and studies supporting product design.
- Develop, modify, evaluate, and verify software components and systems for medical devices.
- Translate user needs into design inputs, specifications, architectures, and component or subsystem designs.
- Analyze complex product-design issues, balance design tradeoffs, and independently evaluate potential solutions.
- Estimate coding time and resources and generate or review requirements, design, architecture, bug, and test documentation.
- Apply design patterns, coding standards, and best practices during code reviews.
- Support software development, integration, deployment, and lifecycle processes.
- Create and refine engineering documentation, including the Design History File, while following design controls, risk management, and quality procedures.
- Collaborate with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams through product launch.
- Support Voice of Customer sessions, apply clinical-procedure knowledge to design inputs, and build relationships across engineering groups.
- Mentor others in industry standards, engineering documentation, design controls, risk management, and medical-device compliance.
Requirements
- Bachelor's degree in Software Engineering, Computer Science, or a related discipline.
- At least 4 years of work experience.
- Knowledge of programming, software component design, design concepts, and design patterns.
- Knowledge of integrated development environments and software analysis tools, including static and dynamic analysis, memory management, and code coverage.
- Knowledge of software development lifecycle, integration, deployment, estimation, and application lifecycle management or traceability processes.
- Knowledge of regulatory and compliance standards applicable to the software development lifecycle.
- Ability to work independently on complex product-design problems and balance component-level design tradeoffs.
- Ability to collaborate across technical, clinical, quality, regulatory, manufacturing, marketing, and project-management functions.
Benefits
- Hybrid work flexibility.
- No travel required.
Categories
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 ● 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 ● 9 consecutive years as one a World's Best Workplace 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