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Stryker

Staff Engineer - R&D(Onsite)

Reposted 8 Days Ago
Be an Early Applicant
In-Office
Irvine, CA, USA
103K-171K Annually
Mid level
In-Office
Irvine, CA, USA
103K-171K Annually
Mid level
The Senior Engineer will collaborate with various teams to drive product development in the medical device industry, focusing on PE thrombectomy devices and ensuring compliance with industry standards.
The summary above was generated by AI
Work Flexibility: Onsite

At Stryker’s Inari Medical, 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 a Senior Engineer - R&D to join our team of passionate innovators and engineers.

To learn more about Stryker’s Peripheral Vascular device portfolio, click here: Stryker PVD

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

  • Collaborate cross-functionally with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams to drive project success with minimal supervision.
  • Support product launches and the qualification of new materials.
  • Work in pre-clinical environments alongside physicians and surgeons to facilitate product development and evaluation.
  • Lead verification and validation activities for new product development, specifically for PE thrombectomy devices.
  • Apply fundamental and advanced engineering principles to solve complex problems; develop and prototype solutions to demonstrate proof of concept.
  • Demonstrate deep understanding of product use, clinical procedures, customer needs, and design inputs to guide development.
  • Ensure compliance with industry standards, regulatory requirements, and design control processes, including risk management and quality system procedures.
  • Independently create and refine engineering documentation, including Design History Files, while managing priorities and ownership of complex tasks.
     
What you needRequired Qualifications:
  • Bachelor’s degree in engineering (Mechanical, Biomedical, or related discipline).
  • 4+ years of experience.
  • Experience in the medical device industry.
  • Hands-on experience or strong knowledge in new product development processes.
  • Proficiency in design and concept generation using CAD tools (SolidWorks preferred).

  


$102,700 - $171,100 USD Annual

  


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.

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