An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing an electronic document system, ensuring compliance with regulatory standards, and supporting audits and inspections. The ideal candidate will have a strong background in document control within a regulated environment, excellent communication skills, and the ability to work collaboratively across departments. Join a dynamic team dedicated to quality and continuous improvement, where your contributions will help shape the future of cell therapy processes.
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