Quality Engineer I LancesoftQuality Engineer IPleasanton, CA$30This role assists senior engineers with validation activities, quality documentation, and problem solving in a highly regulated environment governed by FDA 21 CFR 820, ISO 13485, and ISO 14971. Key Responsibilities Support validation activities Assist in equipment, process, and software validation (including CSV), troubleshoot discrepancies, and help plan validation efforts using risk based approaches.
(US) Edge AI Architect– CUDA / C++ / Computer Vision Codvo.ai(US) Edge AI Architect– CUDA / C++ / Computer VisionSanta Clara, CaliforniaWe are looking for a highly motivated and technically proficient Edge AI Engineer with a strong background in Edge AI devices, computer vision algorithms, and AI model deployment in the MedTech domain. • Bachelor’s or Master’s degree in Computer Engineering, Electrical Engineering, Biomedical Engineering, or related field.
Sr R&D Engineer Russell Solutions GroupSr R&D EngineerFremont, CAResponsible for design and reliability improvements to existing products, development of new products, processes and technologies based on company's core technology, to meet market needs and corporate objectives. Collaborate with Quality to review and analyze complaints, conduct root cause failure mode analysis and maintain Risk Management documentation related to the product design.
NewStaff Quality Engineer, Design Quality - Pleasanton, CA Calyxo IncStaff Quality Engineer, Design Quality - Pleasanton, CAPleasanton, CA$170,000–$185,000 / yearIn This Role, You Will: Ensure design controls for new product development and improvement project activities, including risk management, design V&V, product software validation, design reviews, tagging/tracing, non-product tools validation, test method validation, and design transfer are in compliance with Calyxo Quality System, FDA 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304, IEC 60601, and relevant global regulations. Drive risk management activities per ISO 14971, including risk management plan, hazard analysis, FMEAs (design, software, user), risk-benefit analysis, and risk management report.
Principal Clinical Engineer Imperative CarePrincipal Clinical EngineerCampbell, CA$188,000–$220,000 / yearServe as the subject matter expert when establishing and implementing project plans for product development including preclinical testing, bench testing, model development needs, in-vitro test methods and plans and in-vivo animal studies. What You’ll Do As an expert level professional, the Principal Clinical Engineer will offer subject matter expertise to drive the development and improvement of Telos’ technology to elevate our products clinical application through intuitive design and meaningful improvements for physicians when using our products.
Senior Engineer, Validation and Reliability Apidel TechnologiesSenior Engineer, Validation and ReliabilityFremont, CAContractorThe ideal candidate combines expertise in angiography imaging systems, laboratory operations, radiation safety, and endovascular procedure workflows to support high-quality testing environments that accelerate innovation and support successful product development. Education & special trainings: Associate's or bachelors degree in radiologic technology, Cardiovascular Technology, Biomedical Engineering Technology, or related technical discipline preferred.
NewSenior Quality Assurance Engineer DanaherSenior Quality Assurance EngineerSunnyvale, CA$116,000–$159,500 / yearAddress nonconformities and deviations by performing risk assessments, identifying root causes, conducting failure mode analysis, defining disposition, and supporting effective corrective and preventive actions to prevent recurrence. Serve as the primary Quality Engineering representative on cross-functional teams for new product introduction and manufacturing sustainment, providing strategic input on design control, risk management, and quality compliance.
Medical Imaging Field Engineer - West Zone (Pipeline) Siemens HealthineersMedical Imaging Field Engineer - West Zone (Pipeline)Palo Alto, CARemoteFull timeIt is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.". Physical Requirements: Lifting 50lbs (floor to above waist/head), walking, ladder/stepstool climbing, bending, twisting, sitting work, squatting work, standing work, high-reach, fine grasping manipulation, good vision, and ability to work alone.
Sr Director, Translational Research Scientist - MD/PhD Intuitive Surgical IncSr Director, Translational Research Scientist - MD/PhDSunnyvale, CARemoteFocusing on a portfolio of Class II and III medical devices in the pulmonary space-including next-generation pre-label products-this leader will focus on translating biological and engineering insights into device design, regulatory submissions, and clinical studies. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).
NewPrincipal Hardware Engineer - Fluidics - Pleasanton, CA Calyxo IncPrincipal Hardware Engineer - Fluidics - Pleasanton, CAPleasanton, CA$250,000–$270,000 / yearIndividually contribute to mechanical/electromechanical design for critical fluidics subsystem components and assemblies and provide expert design review of other team-members designs. This role focuses on the design and control of irrigation and aspiration systems, combining pumps, valves, sensors, tubing sets, and embedded software into safe and reliable products.
Staff Manufacturing Engineer - Shockwave Johnson & JohnsonStaff Manufacturing Engineer - ShockwaveSanta Clara, CaliforniaPerforms productivity and costing analyses (e.g., calculate direct labor, time studies& materials costs for new and existing products), providing solutions that improve efficiency and scalability for years to come. The Staff Manufacturing Engineer is responsible for designing, developing, testing, documenting, and implementing processes, tooling, and fixtures for throughout the product lifecycle, from design to production.
Clinical Research Engineer - Future Forward Intuitive Surgical IncClinical Research Engineer - Future ForwardSunnyvale, CACertain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process). U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.
Senior Quality Engineer, Cybersecurity Verily Life Sciences LLCSenior Quality Engineer, CybersecuritySan Bruno, CAGuides software development teams in the creation and maintenance of Design and Development Files (DDFs), including software development plans, verification and validation plans, software requirements specifications, architecture and design documents, design and code reviews, Risk Management Files (RMF), test protocols and reports, and traceability matrices. Experience with AI/ML-enabled medical device products, including familiarity with FDA AI/ML SaMD guidance, predetermined change control plans (PCCP), and post-market performance monitoring for generative AI applications; experience using generative AI tools (e.g., Gemini, Claude, ChatGPT) to enhance quality and compliance workflows is a plus.
NewSenior Systems Engineer Varian Medical Systems IncSenior Systems EngineerPalo Alto, CA$155,900–$214,357 / yearIt is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.". This role is responsible for defining, managing, and verifying system requirements, solving technical system integration challenges, coordinating cross-functional technical activities, and ensuring successful integration of hardware, software, service and manufacturing considerations throughout the product lifecycle.
Staff Quality Engineer, Design Quality - Pleasanton, CA CalyxoStaff Quality Engineer, Design Quality - Pleasanton, CAPleasanton, CA$170,000–$185,000 / yearEnsure design controls for new product development and improvement project activities, including risk management, design V&V, product software validation, design reviews, tagging/tracing, non-product tools validation, test method validation, and design transfer are in compliance with Calyxo Quality System, FDA 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304, IEC 60601, and relevant global regulations. Drive risk management activities per ISO 14971, including risk management plan, hazard analysis, FMEAs (design, software, user), risk-benefit analysis, and risk management report.
Sr. Bioengineer, Preclinical Development In Vivo Pulse Biosciences IncSr. Bioengineer, Preclinical Development In VivoHayward, CA$135,000–$155,000 / yearBioengineer of Preclinical Development is a key technical contributor responsible for independently executing complex preclinical studies, developing experimental models, and supporting engineering and scientific initiatives that advance the CellFX nsPFA platform. The Company's proprietary CellFX nsPFA (nanosecond Pulsed Field Ablation) technology delivers nanosecond pulses of electrical energy to non-thermally ablate cells while sparing adjacent noncellular tissue.
Senior Mechanical Design Engineer Intuitive Surgical IncSenior Mechanical Design EngineerSunnyvale, CACertain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process). U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.
Software Verification Engineer Globus Medical IncSoftware Verification EngineerRedwood City, CAHFX iQ, Nevro's latest innovation, is the first and only SCS System that uses Artificial Intelligence to optimize and maintain pain relief using each patient's response1.Nevro's unique support services provide every patient with an HFX Coach throughout their pain relief journey and every physician with HFX Cloud insights for enhanced patient and practice management.\n \nNevro also recently added a minimally invasive treatment option for patients suffering from chronic sacroiliac joint ("SI joint") pain and now provides the most comprehensive portfolio of products in the SI joint fusion space, designed to meet the preferences of physicians and varying patient needs to improve outcomes and quality of life for patients.\n \nPosition Summary: \n \nThe Software Verification Engineer will play a key role in the development of a Class III implantable Neuromodulation system for pain management, working cross-functionally to help verify firmware, software applications, and whole systems and make sure that all stakeholders are aligned, and requirements and user needs are met.\n \nEssential Functions: \n\n Serves as a technical test lead for verification test efforts, including owning and optimizing system, sub-system, and module verification and validation efforts to ensure complete system coverage, proper tracing and buy-in from cross-functional stakeholders\n \n\n Owns test descriptions and protocols, ensures comprehensiveness of test coverage\n \n\n Designs, develops, updates, executes, and debugs firmware, software, and/or system tests (manual, interactive, automated) and maintains testing metrics.\n The company started with a simple mission to help more patients suffering from debilitating pain and developed its proprietary 10 kHz Therapy, an evidence-based, non-pharmacologic innovation that has impacted the lives of more than 100,000 patients globally.\n \nNevro's comprehensive HFX spinal cord stimulation (SCS) platform includes a Senza SCS system and support services for the treatment of chronic trunk and limb pain and painful diabetic neuropathy.
Staff Clinical Development Engineer - Incubator Intuitive Surgical IncStaff Clinical Development Engineer - IncubatorSunnyvale, CAWorking closely with physicians and cross-functional partners, you will translate clinical and technical insights into structured development plans, drive execution of clinical and preclinical evaluations, and ensure that key risks are identified and resolved. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).
Sr. Clinical Development Engineer - Strategy Intuitive Surgical IncSr. Clinical Development Engineer - StrategySunnyvale, CACertain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process). U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.