• Senior Specialist, Medical Writing

    Edwards Lifesciences (Irvine, CA)
    …portfolio of products across TMTT. The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment to ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
    Edwards Lifesciences (06/11/25)
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  • Senior Embedded Software Engineer

    Abbott (Alameda, CA)
    …development is required. **Preferred Qualifications** + Solid knowledge of regulations for medical device development, (EN460001, ISO13485, FDA) is desirable. + ... preferred + Embedded UI design experience preferred + Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement… more
    Abbott (06/07/25)
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  • Principal RF Electrical Engineer ( Medical

    Abbott (Pleasanton, CA)
    …**years' experience designing, testing, manufacturing or other engineering support** + ** Medical device experience** + Experience working with an electronic ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (04/22/25)
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  • Manager, Global Education - (Remote)…

    J&J Family of Companies (Irvine, CA)
    …to project level budget. Required Qualifications: + Bachelor's Degree. + 3 years of Medical Device or related field experience. + 3 years in cardiac ... & Johnson MedTech, Electrophysiology, is recruiting a Manager, Global Education to join our team remotely in the US....taking technical content provided from various sources such as Medical Science, Marketing, Clinical, Sales, and R&D and applying… more
    J&J Family of Companies (06/11/25)
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  • Territory Manager

    Kestra Medical Technologies, Inc (Bakersfield, CA)
    …Kestra team has over 400 years of experience in the external and internal cardiac medical device markets. The company was founded in 2014 by industry leaders ... by the opportunity to unite modern wearable technologies with proven device therapies. Kestra's solutions combine high quality and technical performance with… more
    Kestra Medical Technologies, Inc (03/26/25)
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  • Software Architect Sr. - Embedded Systems

    Panasonic Avionics Corporation (Irvine, CA)
    …(SOC), operating systems, virtualization, concurrency, virtual memory, caching, interrupts, device drivers, real-time, assembler programming. + 5+ years - Experience ... systems, integration of them into embedded hardware, and experience with device drivers, kernel modules, system calls, and system-level programming. + Embedded… more
    Panasonic Avionics Corporation (04/25/25)
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  • Director, Business Development - Regulatory Drug…

    Cardinal Health (Sacramento, CA)
    …consultants have provided expertise and guidance to help pharmaceutical, biotechnology and medical device companies get their products to market. Our regulatory ... focused on new business development (hunting) within biopharma and medical device companies as well as managing...but not limited to, a candidate's geographical location, relevant education , experience and skills and an evaluation of internal… more
    Cardinal Health (05/21/25)
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  • Clinical Education Specialist - PACE

    Terumo Neuro (Aliso Viejo, CA)
    …**Desired Qualifications** 1. Training and education experience. 2. Experience in medical device industry. 3. Located locally in proximity to Aliso Viejo, ... **12838BR** **Title:** Clinical Education Specialist - PACE **Job Description:** Provide support to the Clinical Education (CE) team, use knowledge and skills in… more
    Terumo Neuro (05/30/25)
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  • Staff Specialist Regulatory Affairs - Hybrid

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …**Overview** As Staff Specialist, Regulatory Affairs, you will develop and implement medical device regulatory strategies to obtain timely approvals from ... Minimum 3 years of practical experience regulatory affairs, with a focus on medical device systems + Knowledge of international regulatory requirements (eg, FDA… more
    BD (Becton, Dickinson and Company) (05/16/25)
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  • Biologics Principal Supplier Quality Engineer

    Hologic (San Diego, CA)
    …process validation test plans, protocols, and reports to ensure compliance with medical device standards. + Validate test methods for verification and ... knowledge of FDA Quality System Regulation, ISO 13485, and Medical Device Regulation. + 5+ years of...(Fishbone, 8D, 5Whys, & CAPA). + Project Management proficiency. ** Education ** + BS or BA degree, preferably in BioMedical… more
    Hologic (03/25/25)
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