• Clinical Research Associate I - Butte Lab…

    Cedars-Sinai (Los Angeles, CA)
    …will be involved in the development and possible commercialization of a novel medical device technology. Interest or experience in a start-up environment with ... will assist in the effort in validating the clinical trial of groundbreaking medical imaging systems. The job will provide an outstanding opportunity to work with… more
    Cedars-Sinai (08/23/25)
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  • Manager, Engineering R&D

    Terumo Neuro (Aliso Viejo, CA)
    …any other related field. 2. Minimum six (6) years of relevant work experience in medical device industry. 3. Minimum one (1) year of management experience. 4. ... functionally with Associates across all departments in R&D, Operations, Quality , and Regulatory Affairs to achieve company...Minimum ten (10) years of relevant work experience in medical device industry. 3. Minimum two (2)… more
    Terumo Neuro (08/28/25)
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  • Staff R&D Engineer - Sustaining

    Stryker (Irvine, CA)
    …components for medical devices while working cooperatively with R&D, Quality , Manufacturing, Regulatory , Clinical, Marketing, and Project Management to ... venous and other vascular diseases through purpose-driven innovation. As a fast-growing medical device company, we develop breakthrough technologies that treat… more
    Stryker (08/29/25)
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  • Lead Clinical Risk Management Analyst

    Abbott (Alameda, CA)
    …+ Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device . + Advanced medical knowledge related to common medical ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (07/19/25)
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  • Inventory and Logistics Technology Associate

    Kelly Services (San Diego, CA)
    …Logistics Technology Associate:** - Join a premier organization in the medical device industry known for its commitment to quality and innovation. - Enjoy ... Associate** to work at **DePuy Synthes** , a leading medical device company, in **San Diego, CA**...-Performing cycle count and inventory reconciliation activities -Assists in regulatory inspection and perform safety and quality more
    Kelly Services (08/29/25)
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  • Clinical Research Manager - JJMT Electrophysiology

    J&J Family of Companies (Irvine, CA)
    …+ Experience with budget planning, tracking and control is required. + Medical Device experience is required. **Preferred Education & Skills/Experience:** + ... successful performance and delivery of project deliverables, on time with high quality . The Clinical Research Manager will be responsible for encouraging strong,… more
    J&J Family of Companies (08/29/25)
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  • Senior Principal Vascular Therapy Development Rep…

    Medtronic (Orange, CA)
    …+ **SR4:** 10 years B2B or Healthcare Sales with 5 years experience selling Medical device or medical capital equipment **NICE TO HAVE- DESIRED/PREFERRED ... to company policies and procedures + Adheres to financial, regulatory , quality compliance standards and requirements. **Influence...+ Thorough working knowledge of medical terminology, medical procedures and the medical device more
    Medtronic (08/15/25)
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  • Chief Software Architect

    Abbott (Pleasanton, CA)
    …secure, high-performing, and regulatory -compliant software systems supporting next-generation medical device platforms and digital health solutions. This ... mindset. Success in this role requires close partnership with product, clinical, regulatory , quality , compliance, security, and engineering teams within R&D to… more
    Abbott (08/20/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Sacramento, CA)
    …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
    Fujifilm (08/11/25)
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  • Manufacturing Process Development Engineer

    Abbott (Pomona, CA)
    …systems. **PREFERRED QUALIFICATIONS:** + Basic knowledge of federal and other regulations governing medical device assembly and design, eg GMP, QSR, ISO and ... Abbott Quality Management System per ISO, FDA, and other regulatory agencies. + Responsible for exhibiting professional behavior with both internal/external… more
    Abbott (08/27/25)
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