Document Control Specialist ISO 9001 & GMP Compliance
Listed on 2026-10-12
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
R3 Lithium in Covington, GA is seeking a Document Control Specialist to manage, track, and maintain engineering and project documentation across the lifecycle, ensuring accuracy and accessibility in accordance with the Management System.
You will administer DMS/eQMS systems, maintain revision histories, support audits, and collaborate with engineering, quality, and operations to meet regulatory standards such as ISO 9001, GMP, and FDA 21 CFR Part 11.
Are you ready to take on the Document Control Specialist for ISO 9001 & GMP Compliance role at R3 Lithium Inc.?
This role, Document Control Specialist for ISO 9001 & GMP Compliance at R3 Lithium Inc., could be your next career step.
We would love to welcome a new Document Control Specialist for ISO 9001 & GMP Compliance to our team in Covington, GA, United States.
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