- Meta (Burlingame, CA)
- …Meta AI and other wearable devices . **Required Skills:** Medical Devices , Verification and Validation Engineer Responsibilities: 1. Develop and ... and Validation Engineer to join our medical devices compliance team, focusing on wearables...sets **Preferred Qualifications:** Preferred Qualifications: 11. Experience working with medical device system verification and/or… more
- Meta (Burlingame, CA)
- …seeking a Product Verification and Validation Engineer to join our medical devices compliance team, focusing on wearables and Software as a Medical ... AI and other wearable devices . **Required Skills:** Medical Devices , System Verification Engineer...to joining Meta 8. 3+ years of experience in medical device system engineering or a related… more
- US Tech Solutions (San Bruno, CA)
- …with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process Verification , and ... + Managing cross-functional or cross-team projects to bring regulated medical device products to market. + Ensuring...audit readiness and regulatory submissions. + Support bringing novel medical devices from concept to release, manage… 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
- Cisco (San Jose, CA)
- Electrical Post Silicon Validation Engineer Apply (https://jobs.cisco.com/jobs/Login?projectId=1445100) + Location:San Jose, California, US + Area of ... Software Development + Job Id1445100 New **Meet the Team:** Welcome to the Post-Silicon Validation Team at Cisco! Our group offers a unique combination of a startup… more
- Abbott (Pleasanton, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... product development experience + Experience working in new product development of medical device industry + Experience leading and influencing other engineers… 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 ... Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation… more
- Meta (Menlo Park, CA)
- …group of researchers and engineers, and use your digital design verification and pre/post-Silicon validation skills/knowledge to drive strategy, planning ... human body. Our chips will enable AR & VR devices where our real and virtual world will mix...and prioritization for testing infrastructure, verification and validation of machine learning Hardware… more
- Abbott (Alameda, CA)
- …to the development, verification , validation , use, and maintenance of medical device software/systems in support of the Quality system. + Coordinate ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....validation , and maintenance of application in support of medical device software. + Software Quality lead… more
- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... discipline. + Must have 5+ experience in Software Quality Assurance. + Knowledge of medical device standards including FDA QSR, ISO 13485, ISO 14971, 21 CFR… more
- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... MATLAB, or similar high level programming language. Previous work in within the medical device space is also highly preferred. **Responsibilities:** * Perform… more
- AbbVie (Pleasanton, CA)
- …successful execution of the Design Control Process for complex electromechanical medical devices containing hardware, software, electrical and mechanical ... experience as a quality engineer or closely related role within a medical device environment. Alternatively, Employer will accept alternate combination of… more
- Teleflex (Pleasanton, CA)
- …Mechanical Engineering, Biomedical Engineering or related major) * Minimum 5 years of experience in medical device industry; or at least 3 years of medical ... and manage test protocols/reports and other aspects of the verification and validation effort. * Maintain sufficient...and FDA QSR. * Prior experience with hand-held disposable medical devices is preferred. The pay range… more
- Teleflex (Pleasanton, CA)
- …methods and Design of Experiments. * Preferred: 5 years of experience in medical device production or product development. * Preferred: Experience with common ... MPs, Design Transfer reports, etc.) * Leading the process verification and validation activities. * Design and...disposable medical device manufacturing processes (eg molding, reflow,… more
- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... development is required. **Preferred Qualifications** + Solid knowledge of regulations for medical device development, (EN460001, ISO13485, FDA) is desirable. +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Demonstrated knowledge and experience in quality assurance for the development of medical devices and/or drug- device combination products. **Preferred ... for: **Job** **Responsibilities:** * Serve as a lead quality engineer for medical device combination product development projects, with a strong emphasis… more
- Teleflex (Pleasanton, CA)
- …* Minimum 5 years related experience working in a new product development, sustaining engineering in medical device industry or at least 3 years of medical ... alter existing test methods * Provide R&D support for verification , qualification, and validation studies on existing...adhesive and thermal bonding and various other processes for medical device fabrication and design is preferred… more
- Abbott (Menlo Park, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... and validate new sensor technologies, associated electrical and mechanical designs for medical device implants and delivery systems in accordance with regulatory… more
- Broadcom (San Jose, CA)
- …including manufacturability and reliability issues with wide-ranging experience in semiconductor device fabrication and operation, device modeling and circuit ... design, test development and execution, device -level reliability failure mechanisms and testing, assembly process development and qualification, design kit… more
- Medtronic (Menlo Park, CA)
- …Inc. located in Menlo Park, CA. Responsible for products in the form of finished medical devices within the Ear, Nose, Throat (ENT) operating unit (OU) by ... 820 Quality System Regulation (QSR), ISO 13485, European Union(EU) Medical Device Regulation (MDR), State of the...Reproducibility (Gage R&R), Attribute Agreement Analysis, and Test Method Validation (TMV). Develop V&V ( verification and … more