- Meta (Burlingame, CA)
- …services, such as Meta AI and other wearable devices . **Required Skills:** Medical Devices , System Verification Engineer Responsibilities: 1. Design ... Verification and Validation Engineer to join our medical devices compliance team, focusing on wearables...to joining Meta 8. 3+ years of experience in medical device system engineering or… more
- US Tech Solutions (San Bruno, CA)
- …align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process ... audit readiness and regulatory submissions. + Support bringing novel medical devices from concept to release, manage... Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management Systems… more
- BD (Becton, Dickinson and Company) (Temecula, CA)
- …planning, performing, and analyzing bench-level engineering tests or research experiments for drug- device combination products and medical devices . The ... team. This position performs technical analyses of drug delivery systems , designs fixturing, develops and validates test methods, and...software such as Minitab and JMP + Knowledge of drug- device combination products and/or medical devices… more
- AbbVie (Pleasanton, CA)
- …Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year ... (QSR), ISO 13485, ISO 14971, MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes & GMP; & + working… more
- J&J Family of Companies (Santa Clara, CA)
- …Development, execution, and documentation of test plans. + Development, execution and functional verification to medical device standards. + Initiate and ... aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease...devices . + Experience with lasers and pulse discharge systems a plus. + Operate as a team and/or… more
- AbbVie (Pleasanton, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- AbbVie (Irvine, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- Actalent (Irvine, CA)
- …THIS IS NOT A SOFTWARE POSITION Looking for hands on IQ/OQ/PQ Validation in Medical Device Candidates MUST HAVE + Bachelor of Science in Engineering or ... and perform validations for current and anticipated projects. + Ensure appropriate systems are in place to evaluate changes to validated/qualified systems ,… more
- Amazon (Sunnyvale, CA)
- …solutions for integration into Amazon's products, services, and operations. The Lead Systems HW Engineer is responsible for system impact assessment and ... a highly skilled and innovative Lead Hardware Engineer to join our Amazon Device Climate Tech Accelerator program. This role will be instrumental in driving the… more
- US Tech Solutions (San Bruno, CA)
- …for medical devices , specifically focusing on Software as a Medical Device (SClient) or low-risk enforcement discretion products. 2. At least 3-5 ... System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation and… more
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