• Principal R&D Project Manager

    J&J Family of Companies (Santa Clara, CA)
    Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... the treatment of calcified plaque. The Principal R&D Project Manager is responsible for product development, resource,...work experience. + 10+ years of experience in the medical device industry including least 5 years… more
    J&J Family of Companies (05/28/25)
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  • Vice President, Product Innovation…

    Danaher Corporation (Sunnyvale, CA)
    …management within the Diagnostics industry or a related field (eg, Medical Device , Pharmaceuticals, Biotechnology, Life Sciences). Specific experience in ... R&D and Clinical & Regulatory Affairs to drive innovation execution by fostering Product Innovation Manager leadership within our NPD core teams. Partner with… more
    Danaher Corporation (04/29/25)
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  • Market Access Manager

    Aston Carter (Valencia, CA)
    …of demonstrated success in market access, pricing, and reimbursement within the medical device industry. Responsibilities + Develop and execute strategies to ... Job Title: Market Access Manager Job Description We are seeking a proven...years in market access, pricing, or reimbursement in the medical device or healthcare industry. + Experience… more
    Aston Carter (06/03/25)
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  • Principal Program Manager (Assay…

    Danaher Corporation (Sunnyvale, CA)
    …degree within the field with preference for 8+ years of related work experience leading product development in the medical device industry. + Prefer 5+ years ... and PMP Certification or equivalent are also preferred. + Experience in the medical device , diagnostic, or life sciences industries, with a significant focus… more
    Danaher Corporation (05/31/25)
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  • R&D Engineering Manager - Neuro

    Medtronic (Irvine, CA)
    …you will lead a team to design and develop life-saving medical device products. Key responsibilities include product development, managing a technical team ... years of managerial experience **Experience** **Needed** **:** + Thorough understanding of medical device industry and regulatory requirements for class II and… more
    Medtronic (05/29/25)
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  • Technical Program Manager , Connectivity

    Meta (Sunnyvale, CA)
    …around the world. We are looking for a talented Software Technical Program Manager with technical expertise in the wireless connectivity space covering the needs of ... building products for the future. **Required Skills:** Technical Program Manager , Connectivity Responsibilities: 1. Closely collaborate with engineering, certification,… more
    Meta (04/12/25)
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  • Sr. Manager , Regulatory Compliance…

    J&J Family of Companies (Santa Clara, CA)
    Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Description:** Johnson & Johnson is hiring for a **Sr. Manager , Regulatory Compliance - Shockwave Medical ** to...programs as needed. Supports the Integration Plan and New Product Introductions as JJRC member. Can act as a… more
    J&J Family of Companies (06/03/25)
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  • Manager , Regulatory Affairs (International…

    J&J Family of Companies (Irvine, CA)
    …of detailed international registration documentation that supports all stages of a medical device 's lifecycle, from initial product registration through ... We are searching for the best talent for a ** Manager , Regulatory Affairs (International Regulations)** to be located in...At least 8+ years of relevant experience in the medical device industry with at least 6+… more
    J&J Family of Companies (06/12/25)
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  • Manager , Regulatory Affairs (IVD…

    Hologic (San Diego, CA)
    …minimum of 8-10 years direct experience in Regulatory Affairs within the IVD or medical device industries. + Master's Degree in biomedical engineering and/or RAC ... Manager , Regulatory Affairs (IVD On-Market/Sustaining) San Diego, CA,...direct experience in Regulatory Affairs within the IVD or medical device industries. + Software/instrumentation experience strongly… more
    Hologic (04/09/25)
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  • Clinical Research Manager

    Envista Holdings Corporation (Brea, CA)
    …of FDA, GCP and ISO guidelines highly preferred. + Basic understanding of medical device product development processes required. **Preferred:** + Ability ... use environment) design validation and creating documentation required by FDA/MDR ( Medical Device Regulation), Standard Operating Procedures, Good Clinical… more
    Envista Holdings Corporation (05/30/25)
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