• 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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  • Student Nurse Clinical Placement

    Fresenius Medical Center (Petaluma, CA)
    …service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. The Nursing student functions as part of ... a safe and clean working environment. Supports the FMCNA commitment to the Quality Enhancement Program (QEP) and CQI Activities, including those related to patient… more
    Fresenius Medical Center (08/29/25)
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  • Senior Process Development Engineer

    Amgen (Thousand Oaks, CA)
    …systems. + Ensure site's process validation business process adheres to global regulatory agency standards, Amgen's quality requirements, other site policies and ... in aseptic processes, technologies and techniques, all in alignment with evolving regulatory expectations and internal quality standards, leading to continuous… more
    Amgen (07/31/25)
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  • Traffic Control Flagger

    Anvil Builders Inc (Sonoma, CA)
    devices : + Direct and guide traffic: + Operate traffic lights or devices : 2. Safety Compliance: + Ensure regulatory compliance: Workers must ensure all ... both the public and private sectors delivering the highest quality outcomes to the client. We are proud to...following guidelines like the Manual on Uniform Traffic Control Devices (MUTCD) in the US, or similar regulatory more
    Anvil Builders Inc (08/08/25)
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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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  • Radiologic Technologist Lead - Department…

    City and County of San Francisco (San Francisco, CA)
    …contrast media, setting up sterile and non-sterile trays, and providing instruments, medical devices and supplies as requested. + Trains student technologists ... state and departmental standards; uses appropriate filters, cones, protective clothing and devices to obtain high- quality images with radiation exposure levels… more
    City and County of San Francisco (07/04/25)
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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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  • Associate Director, R&D

    Terumo Neuro (Aliso Viejo, CA)
    …other related field 2. Minimum five (5) years of relevant work experience in medical device industry 3. Knowledge of and ability to use design/engineering and ... functionally with Associates across all departments in R&D, Operations, Quality , and Regulatory Affairs to achieve company...Minimum eight (8) years of relevant work experience in medical device industry 3. Minimum one (1)… more
    Terumo Neuro (08/13/25)
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  • CQV Engineers/Specialists - Open Applications

    VTI Life Sciences (Los Angeles, CA)
    …engineers looking to accelerate their careers in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support ... Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training,… more
    VTI Life Sciences (06/24/25)
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