• Specialist, Document Management

    West Pharmaceutical Services (Exton, PA)
    Specialist, Document Management Requisition ID: 70948 Date: Aug 1, 2025 Location: Exton, Pennsylvania, US Department: Quality Description: **This is a hybrid ... CFR 820 preferred and + Experience with MasterControl (preferred) or electronic document management systems **Preferred Knowledge, Skills and Abilities** +… more
    West Pharmaceutical Services (08/02/25)
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  • Global Information Security Regulatory

    Bank of America (Denver, CO)
    Global Information Security Regulatory Management Specialist Denver, Colorado **To proceed with your application, you must be at least 18 years of age.** ... grow, and make an impact. Join us! GIS Policy Regulatory Management Specialist represents Global Information Security...the dangers and resulting consequences of illegal and illicit drug use and alcohol abuse. Our Drug -Free… more
    Bank of America (08/09/25)
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  • Manager, QA Document Control

    Catalent Pharma Solutions (Harmans, MD)
    …+ Responsible for implementation, management , and enhancements of an electronic Document Management System (eDMS). **The candidate:** + Bachelor in a Life ... lifecycle of controlled documents, including but not limited to: records management system including version control, document distribution, archival, retrieval,… more
    Catalent Pharma Solutions (07/23/25)
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  • Supervisory Document Automation Specialist…

    Defense Logistics Agency (Loma, ND)
    …regarding this job. Responsibilities Serves as the Branch Chief for Equipment Management Solutions (EMS). The position provides a senior focal point for the ... oversight of contract administration, billing, invoicing, workload planning and management , budget administration and customer service. Collaborates closely with DLA… more
    Defense Logistics Agency (08/03/25)
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  • Sr. Director - Global Regulatory Lead…

    Lilly (Indianapolis, IN)
    … team. The GRL is responsible for the creation and maintenance of the Regulatory Strategy Document (RSD) and ensures local plans, created by the regional ... drug /device clinical development and knowledgefromhealth authorities such as regulatory policies, regulatory precedents, trends, and emerging regulatory more
    Lilly (06/04/25)
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  • Associate, Global Scientific Communications…

    Lilly (Indianapolis, IN)
    …applications). **Primary Responsibilities:** **1. Content Strategy and Execution: Document Preparation, Development and Finalization/ Document Management ... but not limited to, protocols, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing… more
    Lilly (08/09/25)
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  • AD Promo Lead/Associate Director, Americas…

    Chiesi (Cary, NC)
    …FDA OPDP + Experience with Veeva Vault PromoMats and MedComms, Trackwise, or similar document management systems a plus + Demonstrated expertise in regulatory ... guidance documents that impact domestic and international activities related to Regulatory activities. + Interact with senior management , external departments… more
    Chiesi (07/24/25)
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  • Senior Manager, Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Bismarck, ND)
    …Office programs (Word, Excel, PowerPoint, Outlook) and familiarity with electronic document management systems (EDMS). **Competencies** See OPDC Competencies ... strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle regulatory activities in alignment… more
    Otsuka America Pharmaceutical Inc. (06/19/25)
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  • Lead Capital Markets Document Negotiator…

    Wells Fargo (San Francisco, CA)
    …in complex negotiations. + **Deliver Strategic Insights** : Advise senior management on market trends, regulatory developments, and negotiation strategies ... and oversight of a wide range of documentation, ensuring alignment with regulatory requirements, internal risk frameworks, and market best practices. You will serve… more
    Wells Fargo (07/25/25)
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  • Senior Scientist Regulatory Compliance

    Cambrex High Point (High Point, NC)
    … filings. Responsibilities + Provide guidance and input to project teams on regulatory requirements related to document submissions in support of client ... Provide feedback and/or lead project and site risk assessments relative to quality management systems and impact to client projects/ regulatory filings. + Obtain,… more
    Cambrex High Point (07/17/25)
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