Document Control Specialist - ISO 9001 Records Lead

R3 Lithium Inc.; Covington (GA); On-site; USD 60,000 - 85,000; Full time

Job summary

R3 Lithium Inc. Covington, Georgia, United States is seeking a Document Control Specialist to manage engineering and project documentation across the lifecycle, ensuring accuracy, proper revision histories, and regulatory compliance within the company’s management system.

You will administer DMS/eQMS systems, coordinate reviews, and support audits for ISO 9001, GMP, and FDA 21 CFR Part 11, while collaborating with engineering, project management, quality, and operations teams to ensure timely

Qualifications

• Must have 4+ years of document control experience in manufacturing or related technical environments.
• Experience with ISO 9001, GMP, FDA 21 CFR Part 11 or similar requirements.
• Knowledge of document control processes and change management.

Responsibilities

• Maintain document control systems, databases, and electronic filing structures.
• Manage document lifecycle from creation to archiving and revision history.
• Coordinate reviews, approvals, and transmittals between internal teams and external stakeholders.
• Administer DMS/eQMS, configure workflows, permissions, and troubleshoot routing issues.
• Support audits by providing documentation and records as required.
• Ensure compliance with regulatory standards and maintain current document registers.

Skills

Microsoft Office Suite

SharePoint

Document lifecycle workflows

Version control

Organizational skills

Technical writing

Communication skills

Education

Associate or Bachelor’s degree in Quality related field

High school diploma

Tools

AutoCAD

SolidWorks PDM

Aconex

Procore

OpenText

Autodesk Vault

Job description

R3 Lithium Inc. Covington, Georgia, United States is seeking a Document Control Specialist to manage engineering and project documentation across the lifecycle, ensuring accuracy, proper revision histories, and regulatory compliance within the company’s management system.

You will administer DMS/eQMS systems, coordinate reviews, and support audits for ISO 9001, GMP, and FDA 21 CFR Part 11, while collaborating with engineering, project management, quality, and operations teams to ensure timely