Quality Engineer 2 - SinglePort Da Vinci

Intuitive - Sunnyvale, CA

Hiring: Quality Engineer 2 - SinglePort Da Vinci Company: Intuitive Location: Sunnyvale, CA Job Posted Time: 2026-09-09 18:07:41 Target Skills & Keywords : Agile, HBase, TestNG About the job Experience: •2+ years of working experience in Quality •2 years in medical device environment. •3 years of experience in a regulated industry with 1 years in Medical •minimum 2 years in medical device environment. •Minimum 3 years of experience in a regulated industry with 1 years in Medical Required Skills: •Primary Function of Position The Quality Engineer II supports product development and •operations from concept through commercialization and will serve as the core team •member with the cross-functional product development and operations teams. The •Quality engineer will provide support for design control and risk management, Design •for Reliability and Manufacturing, product Development Life Cycle, and Process •Validation. In addition, this position will play an active role to ensure that the developed •products meet quality standards consistent with Intuitive’ s quality processes, while •meeting design control and regulatory requirements. •Essential Job Duties •Support manufacturing and work cross-functionally to resolve technical problems •Work closely with product development teams. •Monitor priorities and tracks progress against schedules; and communicates •status to management. •Provide support in the implementation and policing of GMP, ISO and FDA •requirements. Qualifications: •Required Skills and Experience •Minimum Education: Bachelor’s in engineering or STEM •Advanced degree preferred with 2+ years of working experience in Quality •Engineering or related field, minimum 2 years in medical device environment. •Experience and familiarity with respect to design control and risk management •from early design and development through commercialization. •Demonstrated experience with electromechanical devices. •Experience with medical standards: ISO 13485, ISO 14971 and FDA Quality •System Regulations with a focus on design controls and design optimization. •Able to navigate quality system with minimal oversight on individual projects. •Balanced risk decision making to drive product quality, gain consensus, and work •through technical challenges. •Able to articulate complex information to teams, including management •Required Education and Training •Minimum BS in Engineering or STEM discipline is required. Compensation: •$88,400 •$140,800 Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!