• Compliance Officer

    City National Bank (Los Angeles, CA)
    …gifts and/or entertainment to clients, and other required disclosures * Review employee electronic communications for compliance with regulatory requirements, ... *COMPLIANCE OFFICER* WHAT IS THE OPPORTUNITY? The Compliance Analyst will work to review a variety of employee compliance requests to ensure that they are in… more
    City National Bank (08/07/25)
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  • Quality Assurance Manager

    Kelly Services (Sacramento, CA)
    …controls for appropriateness, completeness and alignment with quality, validation, and regulatory expectations. + Review and approve sampling protocols, risk ... includes ensuring compliance with cGMP regulations, internal quality standards, and applicable regulatory requirements (eg, FDA, EMA, MHRA). The QA Manager will lead… more
    Kelly Services (07/11/25)
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  • Associate Director Quality Assurance

    Takeda Pharmaceuticals (Thousand Oaks, CA)
    By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... you will lead quality oversight to ensure that all products meet applicable regulatory and Takeda quality standards across global markets. You will oversee critical… more
    Takeda Pharmaceuticals (06/11/25)
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  • Medical Staff Coordinator

    The County of Los Angeles (Los Angeles, CA)
    …a timely manner. + Conducts routine internal audits of the review process to ensure compliance with regulatory agencies; assures credential files are ... varies substantially from information contained in the application. + Initiates the review process for updating the department rules and regulations as defined… more
    The County of Los Angeles (06/05/25)
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  • Senior Associate, Submission Operations

    BeOne Medicines (San Mateo, CA)
    …contribute to the implementation of standards, templates, and procedures related to regulatory documents, recommend associated process improvements. + Act as ... types, both paper and electronic and strong experience in the regulatory submission process . + Familiarity with formatting of regulatory submission documents… more
    BeOne Medicines (07/08/25)
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  • Sr. Director, Clinical Development (MD)

    Gilead Sciences, Inc. (Foster City, CA)
    … filing strategy and lead clinical development contributions in the preparation and review of regulatory documents + Provide scientific and clinical leadership ... with phase 3 and 4 PBC studies and global regulatory filings underway or expected, with potential for work...scientific and clinical leadership or oversight in the preparation, review , and interpretation of clinical study data, ensuring high… more
    Gilead Sciences, Inc. (07/24/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Sacramento, CA)
    …the timely coordination and execution of clinical study reports. + Assist in the review of regulatory reports to ensure that reports accurately reflect proper ... of Responsibility** **:** Clinical Operations: + Manage and/or oversee the development process for critical study documents (eg, protocol, amendments, IB, ICF, and… more
    Bausch + Lomb (06/07/25)
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  • Senior Medical Manager, Medical Affairs - Cellular…

    Gilead Sciences, Inc. (Santa Monica, CA)
    …for promotional and educational materials, clinical trial protocols, and regulatory submissions. + Establish and maintain appropriate scientific interactions with ... lymphoma and multiple myeloma on various activities: Field team resources, Medical Review Committee, External grant review / evaluation, vendor management and… more
    Gilead Sciences, Inc. (06/16/25)
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  • Quality Engineer

    Actalent (Santa Clara, CA)
    …presentations on a quarterly basis * Report on quality systems in quarterly Management Review meetings * Prepare and coordinate regulatory filings such as IDE, ... comply with external regulations. * May manage document control process to ensure the process follows internal...meetings on a regular basis and provide assistance with regulatory strategies for various projects * Review more
    Actalent (08/09/25)
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  • Quality Systems Engineer

    Actalent (Irvine, CA)
    …substantiate claims, and training key stakeholders on the newly developed claims process . Responsibilities + Collect and review existing internal documentation ... III Quality Systems Engineer to join our Quality and Regulatory team. This role is critical in ensuring the...and maintain Standard Operating Procedures (SOPs) for the creation, review , and approval of marketing claims. + Collaborate with… more
    Actalent (08/13/25)
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