• 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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  • Director, Product Management , Innovation

    Danaher Corporation (Sunnyvale, CA)
    …the Infectious Disease testing marketplace highly desired. + Demonstrated experience in Product Management in the Medical Device and Diagnostics industry ... System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Director, Product Management , Innovation is responsible for bringing Cepheid's product vision… more
    Danaher Corporation (07/30/25)
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  • Supplier Engineer

    Caldera Medical (Westlake Village, CA)
    …benchmarking, and continuous improvement tools (Lean). * Strong technical skills in risk management and remediation. * Proven ability to create detailed ... The Supplier Engineer is a key member of Caldera Medical 's supplier management team, responsible for driving...? Caldera Medical is a growth stage medical device company dedicated to improving the… more
    Caldera Medical (08/24/25)
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  • Territory Manager

    ZOLL Medical Corporation (Santa Rosa, CA)
    …trusted to protect more than 1M patients at risk of sudden cardiac death. + HFMS (https://cardiacdiagnostics.zoll.com/products/heart-failure-arrhythmia- management ... that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide...Failure Management system) is a non-invasive, patch-based device that monitors pulmonary fluid levels and has been… more
    ZOLL Medical Corporation (06/18/25)
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  • Quality Engineer, Design Control

    Hologic (San Diego, CA)
    …as CE mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management ISO 14971, and other ... risk control measures. + Support design control and risk management activities, review/approve design control and...in the IVD space. + Working knowledge of Quality Management System for Medical Device more
    Hologic (07/03/25)
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  • IT Systems Analyst II - Inari Medical

    Stryker (Irvine, CA)
    Management etc.), and related integrations + Salesforce certification preferred + Medical device or pharmaceutical industry experience preferred + Experience ... systems + Lead project activities to comply with IT risk compliance and change management policies to...Will be identified in Training Plan. Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance,… more
    Stryker (06/28/25)
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  • Sr. Product Security Engineer (San Diego, CA…

    Abbott (San Diego, CA)
    …of medical devices. Your work will support threat modeling, risk assessments, vulnerability management , and regulatory compliance, helping ensure our ... firmware integrity, authentication, and encryption. + Assist in security risk management activities following ISO 14971, IEC...field. + 6+ years of experience in embedded systems, medical device development, or product cybersecurity. +… more
    Abbott (08/01/25)
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  • Director, Quality Engineering - WW IPD

    BD (Becton, Dickinson and Company) (Brea, CA)
    …system-level approach between pumps and sets, including alignment and consistency in risk management files, coordinated change control processes between pumps ... and risk across the platform. + Lead Risk Management activities in compliance with ISO...of progressive experience in Design Quality Assurance within the medical device industry. * At least 6… more
    BD (Becton, Dickinson and Company) (08/28/25)
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  • BMET Cybersecurity Specialist

    Sodexo (Los Angeles, CA)
    …with CMMS systems and asset management best practices. + Experience with medical device configuration, vulnerability patching, and risk assessments. + ... documentation and security guidelines for medical devices. + Conduct technical risk assessments and determine device exposure based on vulnerabilities. +… more
    Sodexo (08/07/25)
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  • Senior Engineer, Quality Manufacturing

    Cordis (Irvine, CA)
    …up to date with regulatory requirements, standards, and guidelines relevant to the medical device industry and ensure that manufacturing processes adhere to ... Engineering, Biomedical Engineering, or a related Engineering field. + 5+ years in medical device production development + Previous experience working in a… more
    Cordis (08/22/25)
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