Joulé
Job Title:
Sr. R&D Engineer - Med Device Location:
Irvine, CA Hours/Schedule:
Monday–Friday, 8 am to 5 pm Compensation:
$40-50/hr Type:
Contract
Overview The Senior R&D Engineer partners with cross‑functional engineering teams to design, develop, and test medical devices from concept through validation. This role focuses on prototyping, test method development, and design verification to support safe, effective, and compliant medical device solutions.
Responsibilities
Collaborate with R&D engineering teams to design and develop medical devices.
Create and validate test methods to support product development and verification activities.
Perform device prototyping and execute functional and performance testing.
Support 3D printing activities and catheter manufacturing processes.
Conduct product specification testing to verify design requirements.
Perform DFMEA activities to identify and mitigate design‑related risks.
Develop and modify device designs using CAD tools, including SolidWorks.
Document test results, design outputs, and validation activities in accordance with procedures.
Apply engineering best practices to ensure product quality, performance, and compliance.
Qualifications
Bachelor’s degree in Engineering or a related technical discipline.
Minimum of 5 years of relevant experience in medical device research and development.
Experience with medical device prototyping and testing.
Experience developing and validating test methods.
Hands‑on experience with 3D printing and catheter manufacturing processes.
Proficiency with CAD tools, including SolidWorks.
Experience performing DFMEA and product specification testing.
Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
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Sr. R&D Engineer - Med Device Location:
Irvine, CA Hours/Schedule:
Monday–Friday, 8 am to 5 pm Compensation:
$40-50/hr Type:
Contract
Overview The Senior R&D Engineer partners with cross‑functional engineering teams to design, develop, and test medical devices from concept through validation. This role focuses on prototyping, test method development, and design verification to support safe, effective, and compliant medical device solutions.
Responsibilities
Collaborate with R&D engineering teams to design and develop medical devices.
Create and validate test methods to support product development and verification activities.
Perform device prototyping and execute functional and performance testing.
Support 3D printing activities and catheter manufacturing processes.
Conduct product specification testing to verify design requirements.
Perform DFMEA activities to identify and mitigate design‑related risks.
Develop and modify device designs using CAD tools, including SolidWorks.
Document test results, design outputs, and validation activities in accordance with procedures.
Apply engineering best practices to ensure product quality, performance, and compliance.
Qualifications
Bachelor’s degree in Engineering or a related technical discipline.
Minimum of 5 years of relevant experience in medical device research and development.
Experience with medical device prototyping and testing.
Experience developing and validating test methods.
Hands‑on experience with 3D printing and catheter manufacturing processes.
Proficiency with CAD tools, including SolidWorks.
Experience performing DFMEA and product specification testing.
Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
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