Senior Medical Device R&D Engineer - 12-Month On-site

Soho Square Solutions

Brea (CA)

In loco

USD 90.000 - 130.000

Tempo pieno

8 ore fa
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Descrizione del lavoro

Global Medical Device Company is seeking a Senior R&D Engineer for a 12-month contract in Brea, CA. You will contribute to infusion preparation and delivery platform development, focusing on test method development, verification testing and design documentation.

Responsibilities include writing test protocols, validating subsystems, and collaborating with quality, regulatory, manufacturing and marketing teams. A BS in engineering and hands-on lab experience are required.

Competenze

  • BS in Mechanical, Materials or Biomedical Engineering.
  • 3 to 8 years of engineering experience (5 years, or 3 years with an advanced degree, is typical).
  • Hands-on work with test protocols, test reports and verification testing.
  • Experience with medical device design control and design documentation.
  • SolidWorks, Pro/E or another CAD tool.
  • Medical device background strongly preferred. Pharma is also considered.
  • Startup experience is a plus.
  • Willingness to get into the lab and do the work.

Mansioni

  • Develop and validate test methods for subsystems and systems.
  • Write test protocols and reports, and run design verification testing.
  • Analyze test data using basic statistics and DOE
  • Support design inputs, feasibility studies and design changes
  • Prepare design documentation for regulatory filings
  • Work with quality, regulatory, manufacturing and marketing teams

Conoscenze

Test protocols
DOE
Design verification testing

Formazione

BS in Mechanical, Materials or Biomedical Engineering

Strumenti

SolidWorks
Pro/E

Descrizione del lavoro

Global Medical Device Company is seeking a Senior R&D Engineer for a 12-month contract in Brea, CA. You will contribute to infusion preparation and delivery platform development, focusing on test method development, verification testing and design documentation.

Responsibilities include writing test protocols, validating subsystems, and collaborating with quality, regulatory, manufacturing and marketing teams. A BS in engineering and hands-on lab experience are required.

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