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Job description
It’s Time to Join Stryker!
Join one of the Fastest-Growing Teams at Stryker!
Be part of something big—join Stryker’s rapidly expanding business unit, where innovative engineering meets life-changing technology. Our cutting-edge capital products are revolutionizing healthcare, and we’re seeking passionate engineers to drive the development of our next-generation solutions. Imagine being part of a project where your work not only shapes the future of medical devices but also brings smiles and relief to healthcare professionals on the front lines. Ready to take on a challenge that makes a difference? Join us, and let’s build the future together!
What You Will Do
As a Senior Staff Design Engineer, you will lead the research, design, development, and validation of mechanical components for medical devices. This role involves close collaboration with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams to ensure successful project outcomes.
Technical Responsibilities:
- You will independently research, design, develop, and validate components, modules, and sub-systems for medical devices.
- You will translate user needs into detailed design inputs and create complex system-level designs with minimal guidance.
- You will lead advanced prototyping and testing efforts.
- You will analyze and resolve complex design issues with independent judgment.
Business Responsibilities:
- You will apply deep knowledge of customer needs, market trends, and competitive offerings to advance product solutions.
- You will author design inputs with a detailed understanding of clinical procedures.
- You will support internal and external Voice of Customer sessions.
- You will demonstrate growing financial acumen in project management.
Medical Device Compliance:
- You will mentor others in applying industry standards, design requirements, and test strategies in compliance with regulations.
- You will lead the creation and refinement of engineering documentation, including the Design History File.
- You will ensure adherence to R&D procedures such as design controls and risk management per the Quality Management System.
General Responsibilities:
- You will collaborate effectively with cross-functional teams to drive project success.
- You will identify and contribute to the improvement of procedures, processes, and technology.
- You will support and lead segments of complex, multifunctional teams to advance projects from concept to launch.
- You will deliver high-quality results with passion, energy, and a focus on meeting business priorities.
What You Need
- Bachelor of Science in Engineering, Mechanical Engineering, Biomedical Engineering, or other related discipline required.
- 6+ years of relevant work experience required.
What We Would Love That You Have (Preferred Qualifications)
You do not need to have ALL of these
- Proficiency in CAD tools (Creo).
- Strong problem-solving and troubleshooting skills.
- Experience in designing mechanical components and systems.
- Solid understanding of mathematics and analytical methods.
- Expertise in performing detailed stack-ups, FMEAs, and writing requirements specifications.
- Ability to design and execute test protocols to ensure designs meet acceptance criteria.