Design Engineer II

Kasmo Global

Job Title: Design Engineer II

Duration: 1+ Year Contract

Job Description

We are seeking a skilled Design Engineer II to join our team in Irvine, CA. This role requires a hands-on mechanical engineer with experience in new product development, especially within the medical device industry. The ideal candidate will have a strong background in catheter design, mechanical design, and the application of core engineering principles in real-world product development scenarios.

Responsibilities

Independently apply engineering principles to analyze and troubleshoot complex systems.
Select and apply appropriate techniques to solve technical issues across projects.
Summarize, analyze, and draw insights from advanced test results.
Design, coordinate, and execute engineering tests and experiments.
Evaluate feasibility and reliability of new products and test methods.
Manage tasks independently with minimal oversight, providing design direction as needed.
Apply deep understanding of customer requirements to influence design decisions.
Provide guidance or mentorship to entry-level engineers and technicians.
Ensure compliance with design control processes as part of Product Realization (Quality Manual).
Contribute to the creation and maintenance of DHF, DMR, and other R&D deliverables in PLM systems.
Work with vendors and identify new partners for component or system development.
Utilize engineering techniques in areas including fluid mechanics, heat transfer, FEA/CFD, and medical device design standards (e.g., Design of Experiments, regulatory compliance).

Requirements

Bachelor's or Master's degree in Mechanical Engineering or a related field.
3-6 years of relevant industry experience (preferably in medical device development).
Proficiency with SolidWorks , mechanical design, and engineering documentation.
Proven experience in new product development and catheter design .
Strong understanding of core mechanical engineering principles.
Familiarity with regulatory standards and design controls in the medical device industry.

Preferred Skills

Experience with FEA/CFD or other simulation tools.
Familiarity with PLM systems for document control (e.g., Agile, Windchill).
Understanding of IP strategy, test method development, and verification/validation procedures.

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Vacancy posted 1 day ago

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