NewSr NPI Manufacturing Engineer Intuitive Surgical IncSr NPI Manufacturing 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.
Technical Support Engineer ScitonTechnical Support EngineerPalo Alto, CaliforniaAs a key member of the Global Service Team, this role works closely with customers and internal teams to diagnose and resolve technical issues, ensure optimal system performance, and deliver an exceptional customer experience. The Technical Support Engineer is responsible for providing expert technical support, troubleshooting, repair, calibration, and installation assistance for Sciton's advanced medical laser systems.
Senior Design Quality Engineer iRhythm TechnologiesSenior Design Quality EngineerSan Francisco, CA$138,000–$180,000 / yearThe Senior Design Quality Engineer serves as a core team member on cross-functional hardware, firmware, stand-alone software product development projects and provide expertise and guidance to the team on design control and risk management. There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist.
Optics and Computer Vision (Systems) Engineer ScitonOptics and Computer Vision (Systems) EngineerPalo Alto, CaliforniaSpearhead optical calibration, illumination design, image quality analysis, and system-level troubleshooting along the various technology pipelines Resolve image distortion errors and alignment failures by systematically analyzing interactions across imaging pipeline subsystems. You’ll collaborate closely with software, hardware, and clinical teams to guide projects through Sciton’s New Product Introduction (NPI) process—turning innovative ideas into real-world products.
Customer Insights Lead Siemens HealthineersCustomer Insights LeadPalo Alto, CAFull 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.". The Customer Insights Lead Lead is responsible for supporting a team that works collaboratively across functions, business lines and geographies, to provide voice of customer insights that assists the Varian Business Areas to achieve its commitment to create a world without fear of cancer.
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.
Sr. Mechanical Engineer -Disposables Stryker CorpSr. Mechanical Engineer -DisposablesSan Jose, CAThis role will focus on injection-molded plastic components and assemblies, including cartridges, cassettes, tubing systems, connectors, sealing interfaces, locking mechanisms, and other flow-control components integrated into electromechanical medical devices. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
Staff Design Quality Engineer iota BiosciencesStaff Design Quality EngineerAlameda, CaliforniaThe DQE is the subject matter expert in design controls, risk management, and product lifecycle quality, collaborating cross-functionally with Engineering, Manufacturing, Regulatory and Clinical teams to deliver safe and effective products to market. This role is ideal for someone who thrives in a dynamic, fast-paced environment and can balance flexibility with structure, guiding teams through complex regulatory requirements while implementing pragmatic, stage-appropriate processes.
Senior Engineer, New Product Introduction (Metrology) Pacific Biosciences of California IncSenior Engineer, New Product Introduction (Metrology)Menlo Park, CA$112,000–$168,000 / yearIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact us at 650-521-8000, or careers@pacificbiosciences.com for assistance. The candidate must have an appetite for solving complex problems requiring holistic evaluation of product factors and actively seek opportunities for improvement based on statistically meaningful, data-driven conclusions.
Staff Supplier Industrialization Engineer Ceribell IncStaff Supplier Industrialization EngineerSunnyvale, CA$142,000–$169,000 / yearThe Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN''s across the country. You will lead NPI industrialization, evaluate and approve engineering solutions across our global vendor manufacturing sites, vendor manufacturing process and capacity post-launch, conduct robust should-cost analyses, and qualify automation systems to scale capacity.
Senior Engineer, New Product Introduction (Metrology) Pacific BiosciencesSenior Engineer, New Product Introduction (Metrology)Menlo Park, California$112,000–$168,000 / yearIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact us at 650-521-8000, or careers@pacificbiosciences.com?subject=Assistance%20With%20Application. The candidate must have an appetite for solving complex problems requiring holistic evaluation of product factors and actively seek opportunities for improvement based on statistically meaningful, data-driven conclusions.
Sr. Clinical Research Engineer - Future Forward Intuitive Surgical IncSr. Clinical Research Engineer - Future ForwardSunnyvale, CAThe Senior Clinical Research Engineer will play a key role in proctoring early-stage feasibility clinical studies, gathering case insights to support technology advancement, identifying and documenting user needs, managing product requirements, assessing clinical risks, and providing design guidance for clinical and commercial design and development. The Senior Clinical Research Engineer will also work with cross-functional teams-including regulatory, quality, clinical affairs, and finance-to shape clinical indications and commercialization strategies, driving the technology from concept to a commercial-ready product.
Principal Software Engineer, Neuroscience Platforms Astera InstitutePrincipal Software Engineer, Neuroscience PlatformsAlameda, CaliforniaBachelor's degree (or equivalent experience) with 12+ years of experience in computer science, electrical engineering, biomedical engineering, neuroscience, physics, or a related field; graduate work or research experience in neuroscience or a related discipline is a plus but not required. Build stimulus presentation and acquisition systems, including VR environments in Unity, Unreal, or comparable frameworks, that synchronize peripheral streams (eye tracking, displays, haptics) with high-throughput neural recording hardware to millisecond precision.
Clinical Effectiveness Consultant III, Clinician Sutter HealthClinical Effectiveness Consultant III, ClinicianSan Francisco, CA$95.11–$133.15 / hourClinical Laboratory Technologist, Diagnostic Medical Sonographer, Medical Dosimetrist, Biomedical Engineer/Bioengineer, Bioinformatics/Biostatistician Specialist, Blood Bank Technologist, Cytotechnologist, Radiation Therapist, Forensic Science Technician, or Registered Health Information Technician). Total compensation considers multiple factors, including, but not limited to a candidate's experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs.
Clinical Effectiveness Consultant Iii, Clinician Sutter HealthClinical Effectiveness Consultant Iii, ClinicianSan Francisco, CA$95.11–$133.15 / hourClinical Laboratory Technologist, Diagnostic Medical Sonographer, Medical Dosimetrist, Biomedical Engineer/Bioengineer, Bioinformatics/Biostatistician Specialist, Blood Bank Technologist, Cytotechnologist, Radiation Therapist, Forensic Science Technician, or Registered Health Information Technician). Total compensation considers multiple factors, including, but not limited to a candidate's experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs.
Cold Chain Packaging Engineer NET2SOURCE INCCold Chain Packaging EngineerFoster City, CAThis position resides within the Packaging Development team with a primary focus on the development, qualification, and lifecycle management of controlled temperature (cold chain) packaging systems (thermal protection systems) to ensure product quality and regulatory compliance across global distribution of our pharmaceuticals and biologics products. B.S. degree in industrial engineering, mechanical engineering, biomedical engineering, chemical engineering, package engineering, or a related scientific field.
Quality Engineer II Viant Medical LLCQuality Engineer IIFremont, CA$121,264–$126,000 / yearSpecific duties include: (1) independently maintaining compliance, monitoring the effectiveness of, and updating Meraqi's Quality Management System (QMS) through SOP and QWI updates; (2) planning and executing sterilization validations using ethylene oxide, gamma and e-beam radiation; (3) monitoring ongoing sterilization process effectiveness for Class II and Class III devices through dose audits and cleanroom monitoring; (4) conducting and evaluating biological risks for Class III implantable devices; (5) providing quality input for reprocessing and cleaning validation of reusable medical devices; (6) providing product development oversight for Class II and III medical devices with focus on Design Control, Change Control, Risk Management, Production and Process Controls; (7) leading as a QA representative in design/phase reviews throughout the product development life cycle and providing critical feedback; (8) designing and implementing Device Master Record (DMR) features such as Manufacturing Process Instructions (MPI), Bill of Materials (BOM), Lot History Records (LHR), risk analyses including Clinical Hazard Analysis (CHA), Failure Modes and Effects Analysis (FMEAs), etc. and Quality Process Instructions (QPI); (9) leading feasibility studies of the design to determine product ability to function as intended; (10) maintaining detailed Design History Files (DHF) of medical devices throughout all phases of the Design Control process; (11) developing, documenting and updating risk analyses through Risk Management Summary Reports (RMSR), Risk Registers, FMEAs and Hazard Analyses (HA); (12) developing and reviewing verification and validation test protocols and reports; (13) creating, classifying and reviewing equipment for process validation activities such as Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ); (14) independently leading the investigation and closure of Corrective Actions and Preventive Actions (CAPA), and Non-Conforming Material Report (NCMRs); (15) developing objective evidence through data collection and statistical analyses to support customer regulatory submissions and related critical activities such as validations; (16) ensuring supplier quality systems meet Meraqi Medical, Inc. requirements; (17) leading training sessions of company employees in Quality System procedures and processes; and (18) providing software quality assurance, reviewing and approving Software Requirements Specifications (SRS), Software Hazard Analysis and Software Architecture Documents (SAD). Must also have 24 months of experience with each of the following: (1) ensuring quality activities are performed in accordance with 21 CFR 820; (2) providing product development oversight for Class II and III medical devices with focus on Design Control, Change Control, Risk Management, Production and Process Controls; (3) conducting and evaluating biological risks for Class III implantable devices; (4) designing and implementing Device Master Record (DMR) features such as Manufacturing Process Instructions (MPI), Bill of Materials (BOM), Lot History Records (LHR), risk analyses including Clinical Hazard Analysis (CHA), Failure Modes and Effects Analysis (FMEAs), etc. and Quality Process Instructions (QPI); and (5) developing objective evidence through data collection and statistical analyses to support customer regulatory submissions and related critical activities such as validations.
Technical Marketing Engineer - Physical AI for Healthcare NVIDIA CorpTechnical Marketing Engineer - Physical AI for HealthcareSanta Clara, CAYou will work alongside our Physical AI, medical imaging, and healthcare AI researchers, engineers, and product teams to demonstrate the latest NVIDIA advancements in MedTech, and partner with the broader TME team covering healthcare AI and smart hospitals to deliver a coherent developer experience across the stack. You will develop video tutorials, technical blog posts, user guides, walk-throughs, demos, developer workshops, and community hackathons that help robotics developers and MedTech engineers adopt and scale Physical AI.
Sr Software Engineer Navigation Intuitive Surgical IncSr Software Engineer NavigationSunnyvale, 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.
Sr. Clinical Development Engineer, MP Instruments (2 Openings) Intuitive SurgicalSr. Clinical Development Engineer, MP Instruments (2 Openings)Sunnyvale, CAU.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. Clinical Development Engineer, Multiport Instruments (CDE) uses their in-depth knowledge of the surgical environment and medical technology to work with design engineers and clinicians to define, develop, and validate the clinical function of new products within our multi-port robotic platforms.