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    Associate Director QA - Oklahoma City, United States - Skills Alliance

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    Description


    I am working with a client in the cell therapy field who are expanding their QA team and looking for an individual with expertise in GCP/GLP to support their QMS.

    The role is on-site in Burlington.


    Experience:
    Bachelor's or Master's degree in scientific or engineering field.
    Minimum 5+ years in progressive quality roles, preferably in biotech or pharma.
    Extensive experience with GLP or GCP regulations.
    Familiarity with FDA inspections and regulatory audits.
    Leadership experience preferred, managing personnel and driving cultural change.


    Responsibilities:
    Expand Quality Management Systems (QMS) within the organization.
    Lead and participate in third-party and regulatory audits.
    Oversee equipment, system, and supplier qualification.
    Develop and revise SOPs, work instructions, and quality documents.
    Drive CAPA, deviation, risk analysis, and change control management processes.


    Reach out to me at or on LinkedIn if this sounds like an interesting opportunity for you or anyone in your network.

    #J-18808-Ljbffr

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