Senior Engineer, R&D Neurosurgical
$77.7k - $129.5kStryker
Work Flexibility: Hybrid
At Stryker were driven to make healthcare better through cutting-edge engineering. As a Senior Mechanical Design Engineer on our Research & Development team you will play an important role in the design development and commercialization of next-generation neurosurgical products and capital equipment. You will contribute to the development of mechanical systems and subsystems solve technical challenges and collaborate closely with cross-functional partners to move products through development and toward launch.
This is an exciting opportunity for a mechanical engineer who has built a strong foundation in product development and is ready to take on greater ownership broaden their technical experience and continue growing within R&D.
To learn more about Strykers Neurosurgical portfolio click here: Neurosurgical Stryker
You will need to live within commuting distance of our Portage Michigan office as you will need to be in the office 3 days a week and can work from home on other days.
What You Will Do
- Research design develop modify and verify mechanical components and modules for medical devices with increasing independence and ownership.
- Translate design inputs into engineering specifications and develop subsystem-level mechanical designs.
- Develop prototypes and evaluate design solutions to validate concepts performance and design improvements.
- Apply mechanical engineering principles and structured problem-solving to identify and resolve technical challenges throughout product development.
- Create and refine engineering documentation including engineering drawings specifications and Design History File documentation in accordance with design control procedures.
- Apply principles such as GD&T tolerance analysis material selection and design for manufacturability to support robust mechanical designs.
- Participate in design reviews risk assessments testing and verification activities as products progress through development.
- Collaborate cross-functionally with R&D Quality Manufacturing Regulatory Clinical Marketing and Project Management to drive project activities and deliverables forward.
- Develop an understanding of product use and clinical procedures to help inform design decisions.
- Support regulatory compliance by following applicable industry standards risk management processes and quality system requirements.
What You Will Need
Required Qualifications
- Bachelor of Science in Mechanical Engineering Biomedical Engineering or a related engineering discipline.
- Minimum of 2 years of relevant engineering experience.
Preferred Qualifications
- Experience with mechanical design and product development including designing mechanical components assemblies or subsystems.
- Experience using 3D CAD tools such as Creo or SolidWorks to create mechanical designs and engineering drawings.
- Working knowledge of GD&T tolerance analysis materials and manufacturing processes.
- Exposure to prototyping design for manufacturability risk assessment/DFMEA testing or design verification.
- Strong communication and problem-solving skills with the ability to collaborate across engineering and cross-functional teams and take ownership of assigned work.
- Experience within the medical device regulated product development or similar product development environment is a plus.
Must be legally authorized to work in the U.S. and not require employment-based sponsorship now or in the future.
United States of America Pay Ranges:
- USN : $77700 - $129500 USD Annual
Required Experience:
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