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    IT Project Lead III - Minneapolis, United States - C4 Technical Services

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    Description
    IT Project Lead III - QMS
    Location: Remote


    IT Project Lead III: A technical representative who can lead the deployment of modules within an eQMS system. Understand system capability, current functionality and configuration by:

    1. Demonstrates the ability to work with limited direction and can prioritize projects independently

    2. Responsible for the global design of systems by providing business analysis, requirements definition, testing, training, and coordination of readiness activities.

    3. Lead the deployment, hypercare, and use of systems in healthcare manufacturing and distribution sites and within healthcare business divisions.

    4. Create and maintain work instructions for systems.

    5. Create and maintain cataloged data for QMS processes.

    6. Support Digital System's strategic projects and continuous improvement efforts.

    Basic Qualifications:
    • Bachelor's degree from an accredited university
    • Demonstrated capability to manage multiple priorities and projects.
    • Minimum [2] years of experience in one or more of the following areas: document management/document change control, quality management system (QMS) support, technical communications.
    • Experience MS Office Suite (Word, Excel, SharePoint, Teams and Outlook.
    • General understanding or familiarity with using an electronic software platform such as SalesForce, ComplianceQuest, or TrackWise.
    • Effective oral and written communication skills; ability to multi-task; and customer-centric mindset to help the business users with questions.
    • Experience supporting a global organization that is part 11 compliant including software validation planning, testing, or defect resolution.
    • Knowledge of SQL and the ability to write and execute queries.
    Preferred Qualifications:
    • Experience using ComplianceQuest software.
    • Experience with SmartSolve.
    • Experience using JIRA/JQL
    • Experience supporting a global organization that is ISO 13485 or ISO 9001 certified (health care or manufacturing).
    • Minimum [2] years of experience in one or more of the following areas: supplier management and supplier corrective action, nonconformance management, CAPA management, audit management or complaint management processes.
    • Values diversity and inclusion as essential to solving problems quickly and embraces differences in people.
    • Works effectively in a team environment.
    • Technical experience in process, product or quality environment.
    • English language skills required.
    #DICE


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