Mechanical Design Engineer, Staff - NPD

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!

Who We Want

Analytical Problem Solvers: Individuals who not only fix issues but also identify root causes, evaluate the best solutions, and recommend comprehensive upgrades to prevent future problems.

Motivated Product Launchers: Professionals who bring strategic vision and execution to the table, ensuring that products are developed and launched with accuracy and efficiency.

Goal-Oriented Developers: Engineers who keep customer needs and requirements at the forefront, delivering safe, reliable, and high-quality solutions.

Curious Learners: Innovators who actively seek out new research and cutting-edge information to stay ahead of industry trends and prepare for what’s next.

Collaborative Partners: Team players who build and leverage cross-functional relationships to integrate ideas, data, and insights, driving continuous improvement across functions.

What You Will Do

As a 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.
• 4+ 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.