Senior Document Control Specialist; ISO/GMP
Listed on 2026-10-18
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Quality Assurance - QA/QC
R3 Lithium is seeking a Document Control Specialist in Covington, GA to manage engineering and project documentation within the company’s management system. You will control, distribute, and archive documents, ensuring accuracy and accessibility across engineering, quality, and operations teams.
You will maintain DMS/eQMS configurations, support audits, and drive continuous improvement of document control processes while adhering to ISO 9001, GMP, and FDA 21 CFR Part 11 requirements.
This position is for the Senior Document Control Specialist (ISO 9001/GMP) role at R3 Lithium.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Document Control Specialist (ISO 9001/GMP) role in the description above.
We appreciate your interest in this position.
Join R3 Lithium and contribute to our ongoing work.
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