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Stryker
Irvine, California; California, Irvine 6001 Oak Canyon STE 100
Source: Stryker careers · View original posting
From Stryker's posting. “We” and “our” refer to the employer.
Work Flexibility: Onsite
At Stryker, we're committed to improving healthcare through cutting-edge medical technologies. As a Staff R&D Engineer within our Peripheral Vascular Division, you will serve as a technical lead on our multidisciplinary Concept Team, driving the development of next-generation catheter-based technologies and electromechanical systems.
You will play a critical role in transforming unmet clinical needs into innovative device concepts, leading hands-on prototyping efforts, and advancing novel technologies through early-stage feasibility and concept development. Partnering closely with physicians, engineering teams, technology suppliers, and strategic collaborators, you will help shape the future of vascular therapies and accelerate the development of breakthrough products for patients and clinicians.
This role is onsite in Irvine, California.
To learn more about Stryker’s Peripheral Vascular portfolio, please click here: Peripheral Vascular | Stryker
Required Qualifications
Bachelor of Science in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Systems Engineering, or a related engineering discipline.
Minimum four years of relevant work experience.
Experience supporting catheter-based medical device development, including catheter technologies, components, design, testing, integration, or related product development activities.
Experience designing and developing mechanical and/or electromechanical assemblies in a regulated product development environment.
Demonstrated experience leading technical projects, prototype development efforts, feasibility studies, or cross-functional engineering initiatives.
Experience translating user needs, clinical insights, or Voice of Customer feedback into engineering requirements and design specifications.
Proficiency in creating engineering drawings and models using GD&T, CAD, and CAE tools, preferably SolidWorks.
Familiarity with medical device design controls, risk management processes, and quality system requirements.
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