• Therapeutic Strategy VP, Rare Disease…

    IQVIA (San Francisco, CA)
    …a significant impact in the field. A strong background in current FDA regulatory expectations and the global landscape in Rare Disease or Pediatrics. Experience in ... from discovery to market. You will oversee preclinical strategy, clinical strategy, regulatory strategy, and commercial strategy, and assess the risk and probability… more
    IQVIA (07/23/25)
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  • Health System Facilities Compliance Manager

    UCLA Health (Los Angeles, CA)
    …State and local codes, as well as all applicable standards and regulatory requirements across Ronald Reagan University Medical Center, Lynda and Stuart Resnick ... and HR- related Federal, State and Local codes, standards and regulatory requirements applicable to critical-care hospitals, MOBs and standalone/offsite clinics in… more
    UCLA Health (07/19/25)
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  • Associate Director, GCOE Learning and Development

    BeOne Medicines (San Mateo, CA)
    …requirements. + Ensure curricula accurately reflect current SOPs, work instructions, regulatory guidance, and process changes. + Monitor training completion and ... training dashboards, metrics, and compliance reports to leadership, QA, and regulatory stakeholders. + Track training key performance indicators and analyze trends… more
    BeOne Medicines (07/19/25)
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  • Senior Medical Director - Sharp Health Plan…

    Sharp HealthCare (San Diego, CA)
    …promote positive community relations. + Assures plan conformance with legal and regulatory requirements. + Assists CMO in continued builds strong partnerships with ... and makes recommendations for updating current polices to meet accreditation and regulatory requirements + Ensures newly updated EHB's are updated and implemented… more
    Sharp HealthCare (07/19/25)
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  • Cloud DevOps Engineer II

    Abbott (Sylmar, CA)
    …our life-changing medical device software. You'll work closely with developers, QA, and regulatory teams to ensure our systems are fast, reliable, and compliant with ... pipelines that support traceability, automated testing, and documentation for regulatory compliance. + Help design, implement, and deploy cloud-based applications… more
    Abbott (07/18/25)
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  • Clinical Risk Specialist RN

    Scripps Health (San Diego, CA)
    …reviews reports and patient data, and collaborates with external licensing and regulatory agencies. Join our patient-focused Quality, Risk & Patient Relations team ... compliance are upheld. Additional responsibilities include supporting privacy and regulatory investigations, environmental safety reviews, patient relations interface and… more
    Scripps Health (07/18/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …review technical reports, protocols, risk assessments, and relevant sections of regulatory submissions (IND, BLA, MAA, etc.) related to downstream processing. + ... Collaborate closely with Upstream MSAT, Validation MSAT, QA, Regulatory , Process Development, Analytical Development, and CDMO technical teams. + Stay current with… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Staff Product Compliance Manager…

    Intuit (San Diego, CA)
    …payment processing (ACH, credit card), electronic fund transfers, and the regulatory landscape impacting money movement, including state and federal money ... communication and interpersonal skills, with the capacity to clearly convey regulatory compliance matters to various stakeholders, including senior management. +… more
    Intuit (07/17/25)
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  • Distribution/Vegetation Management Asset Strategy…

    Southern California Edison (Pomona, CA)
    …strategies are approved internally as well as developing those concepts into SCE's regulatory filings, such as the General Rate Case, Wildfire Mitigation Plan, and ... us build the future? **Responsibilities** + Supports the development of critical regulatory and legislative initiatives to facilitate the execution of the strategic… more
    Southern California Edison (07/17/25)
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  • Senior Director, Global Clinical Development CNS

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the ... + Formulating a rationale to develop the drug in accordance with a clinical and regulatory strategy. + Working with experts and consultants in the field to refine a… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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