• Regulatory Affairs Specialist I

    Abbott (Sylmar, CA)
    …working mothers, female executives, and scientists. The Opportunity We are recruiting for a Regulatory Affairs Specialist I to join our team on-site in Sylmar, CA or ... AZ. As an individual contributor, the function of a Regulatory Affairs Specialist I is to provide support for...products. + General support as needed. + Support key submissions when requested Required Qualifications - . Bachelor's Degree… more
    Abbott (08/20/25)
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  • Senior Regulatory and Litigation Counsel…

    Google (San Francisco, CA)
    …matters with a global docket, including working through resolving multi-jurisdictional regulatory and civil matters. + Experience working with technology companies ... a bias for action and goal to meet the standards of integrity. As a Regulatory and Litigation Senior Counsel Manager, you'll join a US-based team that leads global… more
    Google (09/05/25)
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  • Senior Manager, Strategy

    Cardinal Health (Sacramento, CA)
    …knowledge, and report generation. + Understand brand-to-biosimilars conversions, FDA regulatory dynamics (eg, drug application submissions and approvals), ... action. + Support research to maintain a pulse on product, supplier, regulatory , and market dynamics; understand how industry trends may impact Averon; and… more
    Cardinal Health (08/14/25)
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  • Project Accountant (Public Works, Prevailing Wage,…

    Essel (Walnut Creek, CA)
    …DIR reporting and certified payroll records. + Coordinate timely certified payroll submissions and ensure regulatory requirements are met. Insurance Compliance + ... compliance reports are accurate, timely, and aligned with legal and regulatory obligations. Key Responsibilities Subcontract Management + Review, draft, and manage… more
    Essel (08/11/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Sacramento, CA)
    …teams. Regulatory Interactions: + Prepare and present clinical data to regulatory agencies (FDA, EMA) during IND submissions , clinical study reports, and ... programs, and liaises with Clinical (including Clinical Operations), Biometrics, Regulatory , Early Clinical Development, Pre-clinical research, Medical Affairs and… more
    Sumitomo Pharma (08/14/25)
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  • Specialty Health Plans Auditor III Claims

    LA Care Health Plan (Los Angeles, CA)
    …intended to ensure that LA Care delegates are in compliance with applicable regulatory requirements and LA Care contractual agreements across all lines of business. ... position is responsible for the Department of Managed Health Care (DMHC) claims data submissions for LA Care and its Plan Partners (PPs), and delegates done each… more
    LA Care Health Plan (09/03/25)
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  • Sr Manager, Biostatistics

    Gilead Sciences, Inc. (Foster City, CA)
    …analysis and reporting, document review and data inclusion for NDA submissions of assigned studies by collaborating with cross-functional partners to meet ... input into clinical development documentation, scientific publications and presentations, and regulatory filings. Dependent upon the area of assignment, you may lead… more
    Gilead Sciences, Inc. (08/13/25)
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  • Sr. Specialist, Scientific Operations (Irvine, CA)…

    J&J Family of Companies (Irvine, CA)
    …provide input and support to related functions ensuring the delivery of key regulatory and medical documents. Specifically, the Sr. Specialist will lead the review ... and performance data, draft reports, coordinate approvals, and when applicable manage submissions to the Notified Body. + Perform technical reviews ensuring the… more
    J&J Family of Companies (09/05/25)
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  • Senior GRC - Dev. & Configuration Engineer

    Columbia Bank (Irvine, CA)
    …+ Ensure data quality, consistency, and compliance with security and regulatory requirements. + Create dashboards and reports that provide actionable insights ... development, and integration with external data sources. + Knowledge of applicable regulatory requirements including FFIEC, SOX, PCI DSS, GLBA and HIPAA. **Job… more
    Columbia Bank (09/04/25)
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  • Manager, Data Disclosure & Transparency

    BeOne Medicines (Emeryville, CA)
    …Health Canada PRCI + Facilitates cross-functional team review and approval of transparency submissions on time and within compliance with regulatory and BeOne ... of studies assigned to employees for writing clinical trial disclosure submissions or other transparency activities and ensuring submission compliance + May… more
    BeOne Medicines (08/30/25)
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