Document Control Specialist for ISO 9001 & GMP Compliance

Rippling, Inc.; Covington (GA); On-site; USD 55,000 - 75,000; Full time

Job summary

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.

Qualifications

• 4+ years of document control experience in manufacturing or engineering environments.
• Experience with ISO 9001, GMP, and FDA 21 CFR Part 11 is preferred.
• Familiarity with document control software and change management processes.
• Strong written and verbal communication skills.

Responsibilities

• Maintain document control systems, databases, and electronic filing structures.
• Route, review, approve, publish, and archive documents and revisions.
• Ensure controlled libraries and document registers are accurate and up to date.
• Coordinate document reviews with internal teams and external stakeholders.
• Support audits by providing documentation and records as required.

Skills

Document control

Quality system awareness

Regulatory knowledge

Technical writing

Attention to detail

Project collaboration

MS Office

SharePoint

Education

Bachelor's or Associate in Quality/Engineering/Information Management

Equivalent experience considered

Tools

AutoCAD

SolidWorks PDM

Aconex

Procore

OpenText

Autodesk Vault

ERP systems

Job description

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.