• Principal R&D Engineer - Shockwave Medical

    J&J Family of Companies (Santa Clara, CA)
    Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... and perform product assessments on benchtop, in-situ, and in-vivo to prove and de- risk viability and feasibility of new product designs. + Identify suppliers and… more
    J&J Family of Companies (08/13/25)
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  • Director Biocompatibility

    Abbott (Santa Clara, CA)
    …Summary** Responsible for Biocompatibility support to the research & development of new medical device products as well as the maintenance of business activities ... the existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO...development and provide solutions for the evaluation of safety risk for manufacturing and life cycle management more
    Abbott (07/24/25)
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  • Director R&D Program Management

    Abbott (Pleasanton, CA)
    …cross-functional project teams regarding design control, milestone tracking and delivery, risk management and escalation, regular executive leadership review, ... levels in the organization. + Minimum of ten (10) years' experience in medical device development and/or other highly regulated industry + Previous experience… more
    Abbott (08/13/25)
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  • Advanced Practice Provider (NP/PA), Cardiac…

    Stanford Health Care (Palo Alto, CA)
    …examination, hemodynamic parameters, lab values, diagnostic tests (x-ray, echo, etc.), device parameters. 2. Medical and surgical complications, rejection, ... Rotating - 12 Hour (United States of America) A. Coordinates the management of Adult Heart Transplant, Adult Lung Transplant and Mechanical Circulatory Support… more
    Stanford Health Care (08/08/25)
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  • Sr Design Quality Systems Manager

    BD (Becton, Dickinson and Company) (Brea, CA)
    …Center. + Collaborates with core teams to establish Design Controls and Risk Management implementation strategies in compliance with internal, Industry, and ... maintain a Design Controls training program. + Responsible for Risk Management system. Ensures consistent application of...throughout the world. + Expertise in failure investigation and medical device CAPA process. + Experience in… more
    BD (Becton, Dickinson and Company) (07/12/25)
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  • Process Engineer II (Northridge, CA)

    Medtronic (Northridge, CA)
    …assigned. + Develop & utilize technical & wet lab skills associated with medical device coatings/deposition & relevant fabrication processes + Utilize design of ... methodologies including spray, slot, spin, CVD, PVD, as relevant to medical device or semiconductor industries (ex: MEMS photolithography processes)… more
    Medtronic (08/27/25)
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  • Manager, Project Management

    Edwards Lifesciences (Irvine, CA)
    …we look for (Preferred):** + PMP Certification + Experience working in the medical device industry and/or regulated industry + Experience managing projects ... Make a meaningful difference to patients around the world. Our project management teams support many parts of Edwards, including Engineering, HR, Marketing, IT, and… more
    Edwards Lifesciences (08/29/25)
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  • Mgr., Quality Engineering Management

    Amazon (Sunnyvale, CA)
    …investigates new processes and technologies that could impact the quality of the device , and mitigating these risks through the validation phases. Later the Sr. Mgr. ... with other cross-functional leaders from engineering, reliability, operations and product management throughout all aspects of their work. The successful candidate… more
    Amazon (08/16/25)
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  • Senior Software Quality Engineer, Post Market

    Stryker (San Jose, CA)
    …Market** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SaMD)/Software in a Medical Device (SiMD) to ... you will do:** + Collaboratively ensure compliance with Quality Management System requirements for post-market activities, driving NC/CAPA, and...strong technical skills. + Experience with Software as a Medical Device (SaMD) and Software in a… more
    Stryker (08/27/25)
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  • Staff Specialist Regulatory Affairs (Hybrid)

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …requirements (eg, FDA QSR, ISO 13485, IEC 62304). + Strong knowledge of risk management processes (ISO 14971) and cybersecurity considerations for medical ... Regulatory Affairs, you will have a deep understanding of Risk Based frameworks, Agile SDLC, experience with cross functional...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
    BD (Becton, Dickinson and Company) (08/21/25)
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