• Senior Manager , Global Regulatory

    AbbVie (San Francisco, CA)
    …procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP). This is a hybrid onsite opportunity. The role ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Senior Manager , RA Global Regulatory Strategy, US & Canada position is responsible for the… more
    AbbVie (06/07/25)
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  • Regulatory Affairs Manager

    Alameda Health System (Oakland, CA)
    Regulatory Affairs Manager + oakland, CA + Quality + Regulatory Affairs + Full Time - Day + Business Professional & IT + $61.76- $102.90 + Req ... hospital operations or patient care experience; two years in accreditation/licensing/ regulatory compliance/ quality /performance improvement/patient safety in healthcare;… more
    Alameda Health System (05/10/25)
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  • Regulatory Affairs Manager

    Abbott (Santa Clara, CA)
    …imaging catheters and software, vessel closure devices and peripheral stents. This ** Regulatory Affairs Manager ** position is an onsite opportunity working out ... regulated industry (eg, medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and… more
    Abbott (04/30/25)
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  • Project Manager , Lead Regulatory

    Liberty Utilities (Downey, CA)
    Project Manager , Lead Regulatory Analyst Downey, CA, US, 90241South Lake Tahoe, CA, US, 96150Tahoe Vista, CA, US, 96148 **Our purpose is sustaining energy and ... both the goal outcome and how we achieve it.** **Purpose** The Project Manager will lead various programs and projects, including applications and rulemakings at the… more
    Liberty Utilities (07/01/25)
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  • Sr. Manager , Payor Relations…

    Abbott (Livermore, CA)
    …(https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU ... their health and get on with their lives. This position provides regulatory compliance leadership for the business, ensuring the policies, procedures, and practices… more
    Abbott (07/19/25)
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  • Program Management - Product…

    Applied Materials (Santa Clara, CA)
    …Management Professional (PMP), Program Management Professional (PgMP), and Certified Regulatory Compliance Manager (CRCM) are highly desirable. **Years of ... are seeking a highly skilled and experienced Senior PMO to support our Product Regulatory Compliance program . This critical role ensures our products meet all… more
    Applied Materials (05/10/25)
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  • Regulatory Affairs Project Manager

    Actalent (Irvine, CA)
    Job Title: Regulatory Affairs Project ManagerMUST HAVE + Project management expertise with 6-8+ years of experience. + Experience in medical device industry. + PMP ... to deliver the product on time, within scope, maintaining quality , and adhering to budget constraints. Responsibilities + Manage...and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this… more
    Actalent (07/23/25)
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  • Construction Quality Assurance Specialist-…

    SLAC National Accelerator Laboratory (Menlo Park, CA)
    Construction Quality Assurance Specialist- Program Manager Job ID 6440 Location SLAC - Menlo Park, CA Full-Time Regular **SLAC Job Postings** **Construction ... Quality Assurance Specialist/ Program Manager ** **Position...and regulatory requirements. + Strong understanding of quality program elements including document control, inspections,… more
    SLAC National Accelerator Laboratory (07/02/25)
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  • Quality Patient Safety Program

    Dignity Health (San Bernardino, CA)
    **Responsibilities** The Quality /Patient Safety Program Manager plays a key role in supporting and coordinating quality management (QM), patient safety ... and confidential information while driving continuous improvement in clinical quality , patient safety, and regulatory compliance. **Key Responsibilities:**… more
    Dignity Health (06/06/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Irvine, CA)
    …guidance documents, Medical Device Directive, ISO 14971, ISO 13485, and other global regulatory requirements and quality standards + Detail-oriented + Ability to ... compassionate world. **A Day in the Life** The Sr Regulatory Affairs Specialist will play a key role in...tasks to meet project schedules + Interface with engineering, quality , clinical, marketing, and other functions as needed to… more
    Medtronic (06/10/25)
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