Employer Active
Responsibilities:
Test and/or improve products by developing moderately complex experiments and tests(including writing and executing protocols) analyze results make recommendations and develop reports
Generate and/or modify work instructions test methods engineering drawings/prototypes etc. to establish product and/or process specifications
Create/update portions of design control documents including requirement specs and risk documents
Assign R&D support tasks; gives instruction to technicians on conducting tests; train technicians and
provide feedback; and coordinate technician work
Perform design verification testing
Perform data and statistical analysis and document results
Skills:
Minimum 1 year of experience working with class II or class III medical devices required
Microsoft office suite experience and SolidWorks experience
Experience with design verification and test method validation
Minitab experience highly preferred
Education:
Bachelors Degree in Engineering required
MF ONSITE in Irvine
8am5pm
Approx. 10% international travel based on project
Full Time