Location
Irvine, CA | United States
Job description
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 based on engineering principles
- Generate work instructions test methods engineering drawings/prototypes etc. to establish/characterize 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
- Identify evaluate manage and provide guidance to suppliers including establishing tolerances and defining acceptance criteria for suppliers
Qualifications:
- 1 year medical device experience: Class II or class III
- Writing reports and protocols
- Generate modify(addremove) work instructions
- Test method validation required
- Design verification testing required
- Minitab highly preferred
- SolidWorks experience required
Education:
- Bachelors degree in engineering required
Schedule:
- MF onsite. Usually 8am5pm
- Some travel might be required (10%)
- Contract
* No C2C*
*Must be local to Orange County CA*
Job tags
Salary
