Document Control Specialist

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

Document Control Specialist

R3 Lithium Inc. Covington, Georgia, United States

About this position

R3 Lithium operates North America's first commercial-scale lithium carbonate recovery facility, located in Covington, Georgia. Using a lithium-first extraction process, the company recovers, refines, and returns lithium carbonate from recycled black mass into the battery supply chain for energy storage systems, defense applications, and electric vehicles. Founded in 2026 and privately held, R3 Lithium is headquartered at 9176 Industrial Drive NE, Covington, Georgia. For more information, visit www.r3lithium.com .

The Document Control Specialist is responsible for managing, tracking, organizing, and maintaining various documents including engineering documents, project management document and records throughout the project lifecycle and R3’s Management System documents (policies, procedures, forms, etc.). This role ensures that all documents, engineering drawings, technical specifications, procedures, reports, and project documentation are accurately controlled, distributed, and archived in accordance with company standards and regulatory requirements. The position works closely with various functional areas in the organization including engineering, project management, quality, and operations teams to ensure document control, accuracy and accessibility.

Duties and Responsibilities:

• Maintain document control systems, databases, and electronic filing structures.
• Manage document lifecycle through creation, formatting checks, routing for review/approval, publishing, archival
• Process document revisions and maintain accurate revision histories.
• Manage the receipt, distribution, tracking, storage, and retrieval of engineering and project documentation.
• Ensure engineering drawings, specifications, procedures, and revisions are properly controlled and updated.
• Coordinate document reviews, approvals, and transmittals between internal departments and external stakeholders.
• Verify document compliance with company procedures, quality standards, and regulatory requirements.
• Monitor document workflows and follow up on overdue reviews and approvals.
• Administer document management systems (DMS/eQMS), configure workflows, manage permissions, troubleshoot routing issues.
• Generate and maintain controlled libraries, manage electronic and hard-copy repositories, ensure distribution of current versions and maintain document registers, logs, and status reports.
• Archive completed project documentation according to retention policies.
• Support audits by providing documentation and records as required.
• Assist with implementation and continuous improvement of document control processes and systems.
• Ensure compliance and verify documents meet regulatory standards (ISO 9001, GMP, FDA 21 CFR Part 11).
• Ensure confidentiality and security of sensitive business, engineering and company information.
• Fulfill internal/external requests for records, as approved.
• Collaborate with project teams to ensure timely document submission, revision and distribution.
• High school diploma required; Associate or bachelor’s degree in Quality related field, Business Administration, Engineering Technology, Information Management, or other related field; Equivalent experience may be considered.

Years of Experience:

• 4+ years of document control experience within manufacturing, industrial, engineering, construction, energy, or similar technical environments. Experience supporting industrial, manufacturing, mining, chemical processing, energy, or engineering projects and managing engineering drawings, specifications, and technical documentation, preferred.

Professional Certifications:

• Certifications such as RQAP-GMP or ASQ CQI, preferred.
• Experience with ISO 9001, IATF 16949, or other relevant management systems, required
• Knowledge of ISO 9001, quality management systems, or regulated document control processes.
• Familiarity with AutoCAD, SolidWorks PDM, Aconex, Procore, OpenText, Autodesk Vault, or similar document control software, preferred.
• Understanding manufacturing and engineering change management processes

Skills and Competencies:

• Proficiency with Microsoft Office Suite, including Excel, Word, Outlook, and SharePoint.
• Experience using document management systems (DMS), ERP systems, or electronic document control platforms.
• Knowledge of document lifecycle workflows and version control.
• Understanding of regulatory standards (ISO 9001, GMP, FDA 21 CFR Part 11).
• Strong technical writing, formatting, indexing, and metadata tagging skills.
• Strong organizational skills with exceptional attention to detail.
• Ability to manage multiple projects and deadlines simultaneously.
• Ability to work proactively and collaboratively between multiple business functional areas.
• Excellent written and verbal communication skills.

Physical Job Requirements and Working Conditions:

• This role requires working in a high-volume, fast-paced manufacturing environments and must be able to:
• Perform work primarily in an office environment and requires the ability to operate standard office equipment and keyboards
• Have close visual acuity to perform an activity such as preparing and analyzing documents and drawings, transcribing, viewing a computer terminal and extensive reading
• Walk short distances and up and down stairs
• Support critical manufacturing operations outside of normal business hours, when required