• R&D Engineer

    Medtronic (Santa Ana, CA)
    …and all phases of the Product Development Process (PDP). Responsible for Medical Device Design specifically in Bioprosthetic heart valves, including prototyping ... material, component, and implant level testing to meet development and regulatory requirements. Document design within applicable Design Control, Quality and … more
    Medtronic (07/22/25)
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  • Manager, Mobile Operations

    NBC Universal (Universal City, CA)
    …and mobile service providers globally. + Negotiate wireless service contracts, device leases, and UEM platform agreements with cost, flexibility, and scalability ... including executive and VIP user support through white-glove services and proactive device management. + Oversee incident trends, user satisfaction, and service desk… more
    NBC Universal (09/03/25)
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  • Director Aesthetics Dermal Filler's Pipeline…

    AbbVie (Irvine, CA)
    …years of relevant experience with a successful track record in pharmaceutical and/or medical device marketing - strong analytical and strategic marketing skills ... commercialization for assigned product lines in the Dermal Filler Device Franchise. The Franchise is a key growth platform...the clinical study design as well as into the regulatory strategy. This will be achieved through close collaboration… more
    AbbVie (08/28/25)
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  • Technical Program Manager, Connectivity

    Meta (Burlingame, CA)
    …application 3. Create development, delivery, and compliance schedules based on device requirements, technical challenges, lead-times and business needs provided by ... carrier engineering and WiFi, Bluetooth, regulatory and compliance certification teams 4. Create, collaborate with...setbacks, cutting through ambiguity and driving clarity 9. Drive device prescan and work with compliance team for final… more
    Meta (08/01/25)
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  • Quality Assurance Specialist (Post-Market)

    Hologic (San Diego, CA)
    …equivalent experience. + 3-5 years of experience in post-market quality assurance within the medical device industry such as medical devices, diagnostics, or ... plays a key role in ensuring the safety, effectiveness, and regulatory compliance of medical devices after release. The ideal candidate will be responsible for… more
    Hologic (08/08/25)
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  • Director, Instrument Software

    Abbott (San Diego, CA)
    …+ Minimum 15 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD ... + Minimum 20 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD… more
    Abbott (08/30/25)
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  • Sr Design Quality Systems Manager

    BD (Becton, Dickinson and Company) (Brea, CA)
    …devices marketed in all regions throughout the world. + Expertise in failure investigation and medical device CAPA process. + Experience in medical device ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...+ Lead Quality System auditor experience. + Experience managing regulatory audits and responding to regulatory authorities.… more
    BD (Becton, Dickinson and Company) (07/12/25)
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  • Sr. Manager, Digital Health Technologies Search…

    AbbVie (South San Francisco, CA)
    …science or a related field with relevant experience in pharma, academia, healthcare and/or medical device industries; MBA or consulting experience a plus. + MS ... Purpose AbbVie's Digital Science Team is an innovative group that combines medical knowledge, digital technologies, regulatory , and data science expertise to… more
    AbbVie (08/27/25)
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  • Senior Program Manager - Development Process…

    Medtronic (Northridge, CA)
    …Technical degree is a plus. + Experience with Design Control documentation within medical device industry or Pharma industry. + Experience conducting and ... of initiative and self-motivation. + Prior work experience in a regulated industry ( Medical Device Industry preferred) + Sound experience and through knowledge… more
    Medtronic (09/04/25)
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  • R&D Fellow, Systems Engineering, Interventional…

    Philips (San Diego, CA)
    …solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. ... and thorough manner. + You have experience working in the regulated medical device environment: demonstrating practical knowledge and experience with global… more
    Philips (08/21/25)
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