• Senior Regulatory Affairs Consultant - Labeling…

    Parexel (Sacramento, CA)
    …in SPL (all aspects, types and troubleshooting) and the ability to manage the review and approval of labeling in a document management system. + Electronic ... (XLT), facilitating the development of label updates and enabling senior management review and approval. * Ensure regional labelling compliance with CCDS standards.… more
    Parexel (11/14/25)
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  • Office Engineer

    KDG Construction Consulting (Los Angeles, CA)
    …receipt, distribution, and maintenance of submittals. Perform construction contract correspondence, document and plan control function, input data into Prolog, and ... in Prolog, the project information system. + Maintain project files and document /submittal management systems (hard and electronic copies). To ensure the drawings… more
    KDG Construction Consulting (11/14/25)
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  • Manager III, Facilities Operations And Crafts

    The County of Los Angeles (Los Angeles, CA)
    …contractors, vendors and interested County departments. Reviews or manages the review of plans and specifications and identifies and reports observed design ... correspondence relative to division activities. Reviews or manages the review of work requests and prepares cost estimates and...(7) calendar days of filing your application online. The document should show the date the degree was conferred… more
    The County of Los Angeles (11/07/25)
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  • Supervisor QA

    F & S Fresh Foods (Riverside, CA)
    …for accuracy and compliance. + Monitor/evaluate cleanliness and 5S standards. + Document downtime related problems and corrective actions taken when associated with ... with all management and plant leadership to address and review employee safety or food safety concerns. + Ensure...Conduct a variety of periodic and routine audits to document adherence to company standards, third-party standards, policy, and… more
    F & S Fresh Foods (10/22/25)
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  • Medical Staff Coordinator

    The County of Los Angeles (Los Angeles, CA)
    …Presents completed documents to the Credentialing Committee and Chair for review and recommendation. + Attends Committee meetings and presents completed medical ... staff in a timely manner. + Conducts routine internal audits of the review process to ensure compliance with regulatory agencies; assures credential files are… more
    The County of Los Angeles (12/03/25)
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  • Senior Regulatory Specialist Coordinator,…

    Medtronic (Irvine, CA)
    …may include the following and other duties may be assigned. + Support review of advertising and promotional material to ensure that it meets all medical, ... and regulatory (MLR) process requirements. + Facilitate online and offline review meetings with authors, reviewers/approvers to ensure content approval that supports… more
    Medtronic (11/20/25)
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  • Missile Systems Requirements & Development…

    Northrop Grumman (Los Angeles, CA)
    …+ Coordinate the preparation of system engineering materials during System Requirements Review , System Functional Review , Preliminary Design Review , Critical ... Design Review , System Verification Review , Test Readiness Review , and other program reviews as needed. + Interface with inter-organizational management and… more
    Northrop Grumman (11/20/25)
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  • Construction Disbursement Loan Administrator II

    Columbia Bank (Walnut Creek, CA)
    …the construction loan and the accompanying draws. + Responsible for the review and transaction processing of complex commercial construction loans and draw packages ... active role in team meetings. + Monitor, collect, and review required due diligence items as applicable + Engage...interest reserve advances in the form of an excel document or construction loan management system. + Practice clear… more
    Columbia Bank (11/15/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …to the pharmaceutical environment. **Job Description** + Oversee the capture, review , and dissemination of global regulatory news, public commenting opportunities, ... controlled documents. + Lead weekly regulatory intelligence team meetings to include review and discussion of ad hoc query requests, regulatory background package… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Oncology Early Stage Clinical Scientist (Director,…

    Pfizer (South San Francisco, CA)
    …execution for all FIH programs through proof-of concept + Set the clinical data review strategy, ensure quality data and conduct review of emerging clinical data ... governance bodies, and other internal and external stakeholders + Conduct data review , analysis and interpretation of clinical trials data together with the GDL,… more
    Pfizer (11/08/25)
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