R&D Engineer - Clinical Development(Onsite)

Stryker•Irvine, CA

3d•Onsite

About The Position

At Stryker’s Peripheral Vascular Division, we are transforming the lives of patients suffering from venous and other vascular diseases through purpose-driven innovation. As a fast-growing medical device company, we develop breakthrough technologies that treat life-threatening conditions with speed, safety, and precision. Join us in shaping the future of vascular health. We are currently seeking an R&D Engineer – Clinical Development to join our team of passionate innovators and engineers. Know more about the Division Here: Artix System You will need to live within commuting distance to our 6001 Oak Canyon STE 100, Irvine, CA office. You will need to be in the office 5 days a week.

Requirements

Bachelor’s degree in biomedical engineering , mechanical engineering , or a related engineering discipline.
Demonstrated experience working with anatomical models, clinical imaging, or medical devices in simulated‑use or bench models

Nice To Haves

Demonstrated ability to apply knowledge of materials, manufacturing processes, and mechanical principles to evaluate or support product design.
Ability to communicate basic technical plans, findings, and information clearly to cross‑functional team members.
Experience creating physical models or using model‑fabrication techniques (e.g., molding, 3D printing, machining, or coating).

Responsibilities

Create benchtop models that simulate clinically relevant and challenging use conditions; evaluate device performance with both internal and external stakeholders.
Understand product design features and appropriately select patient anatomy data to support relevant and rigorous device testing.
Challenge and assess novel features of next‑generation devices through structured testing and analysis.
Conduct mechanical characterization of benchtop models to understand performance and behavior under simulated clinical conditions.
With supervision, create or refine engineering documentation—such as Design History File elements—in accordance with company design control procedures.
Learn and apply R&D procedures, including design controls and risk management, in alignment with the Quality Management System.
Support the planning and facilitation of device evaluation sessions, including animal and cadaver testing
With supervision, collaborate cross‑functionally with teams including R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to support project success.