• 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 ... Associates across all departments in R&D, Operations, Quality, and Regulatory Affairs to achieve company objectives and resolve project...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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  • Senior Clinical Data Manager

    GRAIL (Menlo Park, CA)
    …related disciplines is strongly desired. + Experience working on IDE trials and device registries within the medical device and/or pharmaceutical industry. ... a given time. + Experience working with EDC systems. + Knowledge of regulatory requirements (eg ICH, GCP, HIPAA). + Strong interpersonal communication (written and… more
    GRAIL (08/13/25)
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  • Sr. Research Scientist

    Teledyne (Goleta, CA)
    …development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals ... their integration into focal plane arrays. + Assist in device improvements through device design, growth, and...to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high… more
    Teledyne (08/08/25)
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  • Implant Direct Sr. Director, Manufacturing…

    Envista Holdings Corporation (Thousand Oaks, CA)
    …targets and expectations. + 3 years' experience leading operations within a dental device or medical device (FDA regulated industry) environment strongly ... all KPIs, inventory and budget targets + Adhere to and meet all regulatory requirements + Coach, lead and create a culture of continuous improvement utilizing… more
    Envista Holdings Corporation (07/29/25)
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  • Branch Logistics Supervisor - NO CDL

    Owens & Minor (Fresno, CA)
    …success starts with our teammates. Owens & Minor teammate benefits include: + Medical , dental, and vision insurance, available on first working day + 401(k), ... accurate delivery of products. + Ensures staff compliance with all applicable regulatory requirements including, but not limited to, providing documents for the… more
    Owens & Minor (07/27/25)
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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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  • Director, Gher Tmtt Real World Evidence

    Edwards Lifesciences (Irvine, CA)
    …managing multiple RWE projects concurrently-both internally and with consultants-within the medical device , pharmaceutical, or healthcare industry. + Proficiency ... regulatory and payer landscapes, and evidence requirements for medical devices. + Experience engaging with external stakeholders to support evidence-based… more
    Edwards Lifesciences (08/16/25)
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  • Senior Solution Consultant

    Norstella (Sacramento, CA)
    …world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial ... service providers, including the top 10 global pharma and CROs. From drug and device discovery and development to regulatory approval, and from product launch to… more
    Norstella (08/08/25)
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  • Lead Product Security Engineer (R&D Cytology)

    Hologic (San Diego, CA)
    …department in our Diagnostics division is looking for a Security Engineer experienced in medical device and/or instruments security and systems to join our team, ... diagrams. + Collaborate with cross-functional teams (Product Engineering, DevSecOps, Regulatory , Quality) to integrate security into the product lifecycle. +… more
    Hologic (08/22/25)
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  • Project Manager I

    Charles River Laboratories (Northridge, CA)
    …and abilities to perform the job (comparable to 2 years of biotech, medical device , pharmaceutical development, or project management) or equivalent combination ... managing multiple high-impact projects simultaneously. Experience in client communication, regulatory environments, and process improvement is highly desirable. Essential… more
    Charles River Laboratories (08/08/25)
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