Senior Staff R&D Systems Engineer- Electro-Mechanical & Fluidic Systems

Posted 2 Days Ago
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Irvine, CA, USA
In-Office
118K-197K Annually
Senior level
Healthtech • Other • Robotics • Biotech • Manufacturing
Together with our customers, we're on a mission to make healthcare better.
The Role
Leads development of electro-mechanical and fluidic systems for Class II and III vascular medical devices. Responsibilities include system architecture, CAD/CAE modeling, prototyping, sensor-data acquisition, automated verification and validation testing, fixture development, stress testing, design controls, risk management, cross-functional collaboration, technical mentorship, and transferring products from R&D into high-volume manufacturing.
Summary Generated by Built In
Work Flexibility: Onsite

As a Senior Staff R&D Systems Engineer, you will serve as a leading member of the R&D team for our next-generation vascular thrombectomy platforms. This role bridges advanced medical device hardware with high-performance digital ecosystems. You will lead cross-functional project teams through the entire product development lifecycle—independently researching, prototyping, and testing complex fluidic components and electro-mechanical control systems. Additionally, you will actively shape broader R&D organizational initiatives and cross-functional product strategy.

What You Will Do

  • Architect and develop closed-loop fluid control systems driven by real-time sensor feedback and integrated data acquisition architectures.

  • Utilize expert-level CAD/CAE tools to model complex mechanical, fluidic, and electro-mechanical components, producing detailed engineering drawings.

  • Specify functional requirements and evaluate final designs for overall effectiveness, lifecycle cost, system reliability, and clinical safety.

  • Build robust data acquisition frameworks to capture and analyze high-frequency sensor data during R&D testing.

  • Design and lead automated validation and verification (V&V) testing infrastructures, including custom fixture development using LabVIEW or Python.

  • Lead the physical assembly, bring-up, and stress-testing of complex R&D prototypes.

  • Work alongside R&D, Quality, Manufacturing, Regulatory, and Clinical teams to ensure design excellence and optimize components for manufacturing.

  • Drive the seamless transition of New Product Development (NPD) projects into high-volume manufacturing environments.

  • Maintain strict adherence to medical device design controls, risk management, and regulatory frameworks (Class II and Class III).

  • Act as a technical mentor across the division, establishing best engineering practices and identifying process improvement opportunities.

What You Need (Required Qualifications)

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a highly related technical discipline.

  • 6+ years of direct work experience as a systems engineer in the development of Class II and Class III medical devices.

  • Proven track record leading medical device prototyping, verification testing, and cross-functional product strategies.

  • Experience with SolidWorks for complex component modeling and detailed manufacturing drawings.

  • Practical knowledge of closed-loop fluid systems, real-time sensor feedback loops, and data analytics.

  • Familiarity with medical device design controls, risk management frameworks, and strict industry compliance standards.

Preferred Qualifications

  • Project experience applying computational fluid dynamics (CFD) concepts and simulation tools.

  • Advanced hands-on experience with automated testing platforms using LabVIEW or Python.

  • Proven leadership in V&V test automation, custom test fixture development, and NPD design transfer to production.

  • Successful, on-time completion of design transfers from R&D to active manufacturing lines.

  • Precision performance of closed-loop sensor feedback arrays under high-stress fluid dynamics.

  • Increased percentage of automated V&V test cycles, reducing manual prototype testing overhead.

  


$118,000 - $196,600 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.

Skills Required

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a highly related technical discipline
  • 6+ years of direct systems engineering experience developing Class II and Class III medical devices
  • Experience leading medical device prototyping, verification testing, and cross-functional product strategies
  • Experience with SolidWorks for complex component modeling and detailed manufacturing drawings
  • Practical knowledge of closed-loop fluid systems, real-time sensor feedback loops, and data analytics
  • Familiarity with medical device design controls, risk management frameworks, and industry compliance standards
  • Experience applying computational fluid dynamics concepts and simulation tools
  • Advanced hands-on experience with automated testing platforms using LabVIEW or Python
  • Leadership in verification and validation test automation and custom test fixture development
  • Experience transferring new product development designs into production manufacturing lines
  • Experience with closed-loop sensor feedback arrays under high-stress fluid dynamics
  • Experience increasing automated verification and validation test cycles and reducing manual prototype testing

Stryker Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Stryker and has not been reviewed or approved by Stryker.

  • Healthcare Strength Multiple medical plan options with HSA support and global mental‑health access indicate broad, accessible care. These features materially enhance the overall value of the total‑rewards package.
  • Retirement Support A meaningful 401(k) company match with potential additional company contribution, alongside an ESPP, supports long‑term savings and wealth building. Documented plan specifics help employees understand eligibility, timing, and vesting mechanics.
  • Parental & Family Support Paid parental and caregiver leave, adoption and surrogacy assistance, and practical supports like breast milk shipping reflect a comprehensive, family‑friendly approach. These offerings address varied family‑building paths and caregiving needs.

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The Company
HQ: Portage, MI
51,000 Employees
Year Founded: 1941

What We Do

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 130 million patients annually. More information is available at www.stryker.com. Together with our customers, we are driven to make healthcare better.

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