Calibration, County Ordinances, Data Collection, GMP (Good Manufacturing Practices), ISO (International Organization for Standardization), Medical Equipment, OEM (Original Equipment Manufacturer), Presentation/Verbal Skills, Product Development, Quality Engineering, Reporting Skills, Research & Development (R&D), State Laws and Regulations, Test Plan/Schedule, Testing, Writing Skills
No C2C or 3rd Party Candidates will be considered
Must sit onsite in Tustin, CA
Medical Device experience highly preferred
Target pay is $40 per hour W2
Key requirements:
- Ability to follow verbal and written instructions.
- Follow safety guidelines and utilize appropriate safety devices when performing all tasks that require such precautions.
- Coordinate and execute equipment Installation Qualification and Calibration.
- Perform engineering tests per ISO guidelines in support of design qualifications.
- Perform hands-on Tests, data collection, report writing, equipment qualification, and additional R&D support
- General laboratory maintenance.
- Developing new test systems and improving existing test systems together with R&D teams
- Assist in the transfer of newly developed products from OEM R&D to production.
- Perform job functions in accordance with applicable GMP and ISO guidelines.
All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance.