Description: Summary of Job Purpose: Support new product development for Schematic Capture, PCB Layout and Component Engineering. Essential Duties and Responsibilities: Perform schematic capture, symbol & footprint creation, component...
Description: Summary of Job Purpose: Support new product development for Schematic Capture, PCB Layout and Component Engineering. Essential Duties and Responsibilities: Perform schematic capture, symbol & footprint creation, component...
Location: Irvine CA, 92606 Duration: 09+ months Payrate: $50/hr. - $53hr. on (W2) Summary of Job Purpose: Support new product development for Schematic Capture, PCB Layout and Component Engineering. Essential Duties and Responsibilit...
Location: Irvine CA, 92606 Duration: 09+ months Payrate: $50/hr. - $53hr. On (W2) Summary of Job Purpose: Support new product development for Schematic Capture, PCB Layout and Component Engineering. Essential Duties and Respon...
outdoors and a desire to protect it for future generations. Role Summary We are seeking an experienced product designer... on Rivian’s website with a focus on product stories and commerce flows. As a designer on our web team you’ll be responsible...
outdoors and a desire to protect it for future generations. Role Summary As a Lead CMF Designer at the Rivian Design Studio... and conducting employment, background and reference checks; (iii) establishing an employment relationship or entering...
and recruitment process, including assessing you and your application and conducting employment, background and reference checks; (iii...; and (iii) Rivian’s service providers, including providers of background checks, staffing services, and cloud services. Rivian...
Designer for schematic development, PCB layout, and fabrication documentation. Experience in a regulated industry, preferably... with Class II or III medical devices Working knowledge of ISO 13485, ISO 14971, and FDA Quality System Regulations Familiarity...
Designer for schematic development, PCB layout, and fabrication documentation. Experience in a regulated industry, preferably... with Class II or III medical devices Working knowledge of ISO 13485, ISO 14971, and FDA Quality System Regulations Familiarity...