R&D Engineer - Clinical Development(Onsite) at Stryker - Poland

Irvine, California, United States -

Full Time

Start Date

Immediate

Expiry Date

29 May, 26

Salary

144200.0

Posted On

28 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Benchtop Modeling, Device Performance Evaluation, Anatomy Data Selection, Structured Testing, Mechanical Characterization, Engineering Documentation, Design History File, Design Controls, Risk Management, Animal Testing, Cadaver Testing, Cross-functional Collaboration, Biomedical Engineering, Mechanical Engineering, Materials Knowledge, Manufacturing Processes

Industry

Medical Equipment Manufacturing

Description

Work Flexibility: Onsite 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. What You Will Do 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. What You Need Minimum Qualifications 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 Preferred Qualifications 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). $69,500 - $144,200 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. Travel Percentage: 10% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

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Responsibilities

The engineer will create benchtop models to simulate clinical conditions and evaluate device performance with stakeholders, while also challenging next-generation device features through structured testing and analysis. Responsibilities include conducting mechanical characterization, refining engineering documentation under supervision, and supporting planning for device evaluation sessions like animal and cadaver testing.