Principal Quality Engineer - Design Assurance (Npd) Imperative CarePrincipal Quality Engineer - Design Assurance (Npd)Campbell, CA$173,000–$192,000 / yearWhat You'll Bring - minimum requirements for this role: Bachelor's degree in Engineering, Life Sciences, Microbiology, Biomedical Engineering, or related technical discipline with 12+ years of progressive experience in medical devices or regulated industries; or equivalent combination of education and experience. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates.
Senior Quality Engineer Willow InnovationsSenior Quality EngineerMountain View, CaliforniaThe Senior Quality Engineer will participate in the implementation and maintenance of QSR (21 CFR 820) and ISO 13485: 2016 quality systems and qualification activities of Willow Innovations medical breast pump products and non-medical consumer products in support of the Company’s development, manufacturing, quality, regulatory, and clinical affairs efforts. Regulatory Knowledge: Strong understanding of ISO 13485, FDA 21 CFR Part 820 & Part 11, EU MDR, ISO 14971 (Risk Management), ISO 10993-1 Biocompatibility, FDA/EU/UK Food Safe Regulations, WERCSmart, RoHS compliance.
Sr. Clinical Development Engineer, MP Instruments (2 openings) Intuitive Surgical IncSr. 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.
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. Machine Learning Engineer, Medical Imaging Intuitive Surgical IncSr. Machine Learning Engineer, Medical ImagingSunnyvale, 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.
Staff Software Engineer Embedded UI Intuitive Surgical IncStaff Software Engineer Embedded UISunnyvale, 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 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.
Technical Marketing Engineer - Physical AI For Healthcare NvidiaTechnical 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 - Build and Release Intuitive Surgical IncSr. Software Engineer - Build and ReleaseSunnyvale, 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.
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.
Senior Bioinformatics Software Engineer F. Hoffmann-La Roche LtdSenior Bioinformatics Software EngineerSanta Clara, CA$145,300–$269,800 / yearYou will be part of a team working in a fast paced environment, developing cutting-edge, distributed, scale-out Next-Generation Sequencing data analysis software to ensure the highest possible software quality for gene sequencing research and disease diagnostics. You will navigate and contribute to a large code base, applying your knowledge of advanced bioinformatics techniques (such as alignment methods and other sequence analysis algorithms) and neural nets to continuously improve the quality and feature sets of the software products.
Senior Quality Engineer Willow PumpSenior Quality EngineerMountain View, CA$180,000–$200,000 / yearJob Overview: The Senior Quality Engineer will participate in the implementation and maintenance of QSR (21 CFR 820) and ISO 13485: 2016 quality systems and qualification activities of Willow Innovations medical breast pump products and non-medical consumer products in support of the Company's development, manufacturing, quality, regulatory, and clinical affairs efforts. Regulatory Knowledge: Strong understanding of ISO 13485, FDA 21 CFR Part 820 & Part 11, EU MDR, ISO 14971 (Risk Management), ISO 10993-1 Biocompatibility, FDA/EU/UK Food Safe Regulations, WERCSmart, RoHS compliance.
Senior Test Engineer Intuitive Surgical IncSenior Test EngineerSunnyvale, CAThe Senior Test Engineer will work with a team of dedicated individuals within a product development team to assure the quality of new designs, to identify issues related to new designs and processes, and to work with other Test Engineers to develop harmonized test methods. 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).
Senior Electrical Engineer, Medical Devices Abbott LaboratoriesSenior Electrical Engineer, Medical DevicesPleasanton, CA$90,000–$180,000 / yearDemonstrated history of two or more of the following: Releasing to production an electro-mechanical design with design-responsibility of the MCAD, Design of radio frequency antenna elements (modelling and characterization of antennas - preferably low frequency), Use of automation for characterization and/or data analysis to spead design cycles, The translation of electrical requirements into circuit designs and specifications. The Senior Electrical engineer will be primarily working on the CardioMEMS HF system, which remotely monitors changes in pulmanry artery (PA) pressure, an early indicator of the onset of worsening heart failure, to aid physicians in preventing worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients.
Senior Electrical Engineer, Medical Devices AbbottSenior Electrical Engineer, Medical DevicesPleasanton, CaliforniaDemonstrated history of two or more of the following: Releasing to production an electro-mechanical design with design-responsibility of the MCAD, Design of radio frequency antenna elements (modelling and characterization of antennas – preferably low frequency), Use of automation for characterization and/or data analysis to spead design cycles, The translation of electrical requirements into circuit designs and specifications. The Senior Electrical engineer will be primarily working on the CardioMEMS HF system, which remotely monitors changes in pulmanry artery (PA) pressure, an early indicator of the onset of worsening heart failure, to aid physicians in preventing worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients.
Senior Manufacturing Quality Engineer EBR Systems IncSenior Manufacturing Quality EngineerSunnyvale, CA$115,600–$156,400 / yearSupporting production by troubleshooting issues and improving yields, collaborating with contract manufacturers to resolve issues, closing non-conforming material reports promptly, and ensuring adherence to internal procedures are crucial. Ability to work independently, using good judgment, initiative, and analytical abilities, to accomplish short and long-range projects, anticipate likely needs, and recommend actions with minimal direction.
Field Service Engineer - California Bay Area Becton Dickinson and CoField Service Engineer - California Bay AreaSan Jose, CA$35–$40 / hourAssociate's degree in Electronics, Mechanical, Robotics, or Biomedical Engineering Technology preferred, plus 3-5 years field service experience (or equivalent combination of education and relevant experience). For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance.
Senior Clinical Development Engineer Capstan MedicalSenior Clinical Development EngineerSanta Cruz, CaliforniaBased in Santa Cruz, our unique workspace blends cutting-edge Bay Area innovation with a lifestyle-driven environment near trails, beaches, and open space—creating the perfect place to do meaningful, career-defining work. Our team combines surgical robotics, catheter-based delivery, and next-generation implants to transform complex procedures into safer, lower-stress solutions for patients and clinicians alike.
Sr. Field Service Engineer Countable LabsSr. Field Service EngineerPalo Alto, CAThe Field Service Engineer (FSE), along with the Field Application Scientists (FAS) are the primary technical point of contact for customers using the Countable PCR platform, responsible for on-site installation, preventative maintenance, and troubleshooting of Countable instruments as well as the third-party equipment that support the workflow. You will travel to customer laboratories to install and qualify new systems, perform scheduled maintenance, diagnose and resolve instrument and software technical issues, and represent Countable Labs' commitment to reliability and customer success.
Staff Systems Engineer - Pleasanton, CA CalyxoStaff Systems Engineer - Pleasanton, CAPleasanton, CA$195,000–$205,000 / yearYou will define and own the end-to-end system architecture , translate user and business needs into robust system and subsystem requirements, validate architectural decisions through prototyping and bench testing, and proactively de‑risk critical technical challenges. The ideal candidate combines hands-on medical device experience , strong systems thinking , and the technical leadership expected of a staff-level engineer operating across hardware, software, disposables, and clinical use environments.