• Veeva QMS Organizational

    CGI Technologies and Solutions, Inc. (Cambridge, MA)
    ** Veeva QMS Organizational Change Manager** **Category:** Testing/Quality Assurance **Main location:** United States, Massachusetts, Cambridge **Position ... Description:** We are seeking an experienced Organizational Change Management (OCM) Lead to support the Veeva... Change Management (OCM) Lead to support the Veeva QMS Implementation within a global pharmaceutical… more
    CGI Technologies and Solutions, Inc. (02/14/25)
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  • Sr. Principal - Deviation Mentor

    Lilly (Concord, NC)
    …actions and timelines. + Act as the Power User and Site Instructor for the One QMS Veeva system, covering deviations, change controls, and CAPA. + Author and ... One QMS Responsibilities + Manage the transition of the Quality Management System ( QMS ) from the TrackWise platform to Veeva for the CONCORD site. +… more
    Lilly (02/07/25)
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  • Director, R&D Process Quality Business…

    Amgen (Washington, DC)
    …and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Trackwise. + Thorough understanding of ... Analytics** **What you will do** Let's do this! Let's change the world! In this vital role you will...and the generation of quality metrics to help Amgen's QMS function effectively and efficiently, while improving continuously as… more
    Amgen (01/31/25)
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  • Senior Manager, R&D Quality Operations…

    BeiGene (San Mateo, CA)
    …MSOffice skills (Outlook, Word, Excel, PowerPoint, Project) + History of working with Veeva QMS System is preferred **Communication & Interpersonal Skills** + ... improvement efforts, and driving process enhancements through digital innovation and change management. The Senior Manager will ensure cross-GxP strategic alignment… more
    BeiGene (02/15/25)
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  • Document Control Specialist

    Actalent (Parsippany Troy Hills, NJ)
    …documents process in the DMS to support business initiatives. + Administer REAL and Veeva EDMS, including the periodic review process. + Ensure proper EDMS to LMS ... computer competencies. + Attention to detail. + Multi-level communication skills. + Organizational skills. + Time management skills. + Quality System (QS) document… more
    Actalent (02/25/25)
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  • Sr. Clinical Trial Assistant - Durham, NC

    Kedplasma (Fort Lee, NJ)
    …following areas, as indicated below: 40% Clinical trial support 30% Veeva management including training 20% Project management support 10% US functional/departmental ... Perform administrative Trial Master File (TMF) management and maintenance activities in Veeva 's eTMF system. 4. Instruct and train clinical team and/or delegated… more
    Kedplasma (01/25/25)
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  • Executive Director, Clinical Quality Assurance

    Vera Therapeutics (Brisbane, CA)
    …* Experience with planning and conducting GCP focused audits preferred. * Proficient in Veeva QualityDocs and Veeva QMS . * Demonstrates proven track record ... target the source of immunologic diseases in order to change the standard of care for patients. Vera's lead...and multi-task successfully in a fast-paced environment. * Excellent organizational skills and attention to detail are essential. Vera… more
    Vera Therapeutics (02/07/25)
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  • Global Quality Excellence Lead

    Abbott (Alameda, CA)
    …cross-functional collaboration, and data management, while handling various types of change orders and documentation to maintain compliance and support ... organizational goals. Ensuring that these systems are aligned with...production planning, process validation, and quality control. + Engineering Change Management: Automate change workflows, establish review… more
    Abbott (12/28/24)
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  • QA Representative - Contract Manufacturing

    Lilly (Indianapolis, IN)
    …provides assistance and guidance on deviation investigations, CAPA, change control, batch release, equipment qualification, process validation, audits, ... for CMs process manufacturing including: protocols, technical reports, deviations, change controls, inspection procedures and specifications, sampling plans, sort/rework… more
    Lilly (01/24/25)
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