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Document Control Manager Jobs in Suwanee, GA (NOW HIRING)

C.W. Matthews

Asphalt Quality Control Technician

Atlanta, GA · On-site

$18 - $23/hr

... C Manager. * Collect samples of materials and asphalt for testing and analysis. * Record and report data collected from tests to ensure accurate tracking and documentation. * Assist in the ...

Sysco

Quality Control Associate

Atlanta, GA · On-site

RESPONSIBILITIES Provide technical, customer relations, and personnel management for major programs ... Inspect inbound freight, warehoused product, and/or outbound product and document product condition ...

Fulgent Therapeutics

Quality Manager

Alpharetta, GA · On-site

Document control * Corrective Action / Preventative Action (CAPA) * Safety practices * PHI / PI (Confidentiality) * Provide direction and management oversight for QMS activities including (but not ...

Faithtechnologies

QC Electrician

Atlanta, GA · On-site

Identify potential quality issues from review of construction documents. * Analyze startup ... Provides guidance to field employees, project supervisors, and management on matters concerning job ...

Shimizu North America

Project Manager

Atlanta, GA · On-site

Effectively manage the document control process and insure constant communication with the client and both internal and external Design Team members. * Manage all financial aspects of the project ...

Shimizu North America

Project Manager

Atlanta, GA · On-site

Effectively manage the document control process and insure constant communication with the client and both internal and external Design Team members. * Manage all financial aspects of the project ...

Faith Technologies

QC Electrician

Atlanta, GA

Identify potential quality issues from review of construction documents. * Analyze startup ... Provides guidance to field employees, project supervisors, and management on matters concerning job ...

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Showing results 41-60

All JobsDocument Control JobsDocument Control Manager JobsDocument Control Manager Jobs in Suwanee, GA

Document Control Manager information

See Suwanee, GA salary details

$32.6K

$92.1K

$147.1K

How much do document control manager jobs pay per year?

As of Aug 13, 2026, the average yearly pay for document control manager in Suwanee, GA is $92,090.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,900.00 and $109,800.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a document control manager?

To thrive as a Document Control Manager, you need deep knowledge of document management processes, attention to detail, and often a degree in business administration or a related field. Familiarity with document management systems (DMS) such as SharePoint, Aconex, or similar platforms, along with certifications like ISO 9001, is typically required. Strong organizational skills, effective communication, and the ability to lead teams set top performers apart. These competencies ensure accurate, secure, and efficient handling of critical documents, supporting compliance and smooth project workflows.

What is a document control manager?

A document control manager oversees document management systems in an organization, often in design, construction, or engineering fields. As a control manager, you track, file, update, and destroy documents as appropriate. You use a database or filing system to manage confidential business and client documents. Your responsibilities include running software for document maintenance, following procedure requirements for confidentiality and accuracy, and improving processes. Your duties may involve supervising a team of employees, establishing databases, assigning projects, and ensuring compliance and quality control. Qualifications include experience in document management systems, industry knowledge and skills, and for some jobs, a college degree.

Is document control a good career path?

A career as a Document Control Manager involves overseeing the organization, accuracy, and accessibility of company documents, often requiring skills in document management software and attention to detail. It can offer stable employment opportunities in industries like construction, manufacturing, and engineering, with potential for advancement into project management or quality assurance roles.

What are some common challenges a document control manager may face when implementing new document management systems within an organization?

Document Control Managers often encounter challenges such as resistance to change from staff, integrating new systems with existing workflows, and ensuring data security and compliance with industry regulations. Successfully overcoming these hurdles typically involves providing thorough training, clear communication about the benefits of the new system, and collaborating closely with IT and other departments. Additionally, establishing standardized processes and regular audits can help maintain consistency and quality in document management practices.

What is the difference between Document Control Manager vs Document Coordinator?

AspectDocument Control ManagerDocument Coordinator
ResponsibilitiesOversees document management systems, ensures compliance, manages teams, and implements proceduresAssists with document preparation, updates, and distribution under supervision
CredentialsTypically requires a degree in engineering, management, or related field; certifications like ISO or document control certifications are commonOften requires a high school diploma or associate degree; certifications are less common
Work EnvironmentIndustrial, construction, engineering, or manufacturing settingsOffice-based, supporting project teams in various industries

The Document Control Manager holds a leadership role with strategic responsibilities, while the Document Coordinator provides operational support. Both roles are essential for effective document management but differ in scope and seniority.

More about Document Control Manager jobs
What are the most commonly searched types of Document Control jobs in Suwanee, GA? The most popular types of Document Control jobs in Suwanee, GA are:
What are popular job titles related to Document Control Manager jobs in Suwanee, GA? For Document Control Manager jobs in Suwanee, GA, the most frequently searched job titles are:
What job categories do people searching Document Control Manager jobs in Suwanee, GA look for? The top searched job categories for Document Control Manager jobs in Suwanee, GA are:
What cities near Suwanee, GA are hiring for Document Control Manager jobs? Cities near Suwanee, GA with the most Document Control Manager job openings:
Document Control Manager jobs near you
Infographic showing various Document Control Manager job openings in Suwanee, GA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $92,090 per year, or $44.3 per hour.

Quality Manager

SoftWave Tissue Regeneration Technologies

Marietta, GA • On-site

Full-time

Posted 6 days ago

Job description

Position Overview:
The Quality Manager will lead the company's Quality Management System (QMS) and compliance infrastructure
to ensure ongoing adherence to applicable medical device quality and regulatory requirements, including ISO
13485 and FDA Quality System Regulations / QMSR.
This role will own the quality system framework, supplier quality oversight, CAPA administration, audit readiness,
and regulatory support activities, while working cross-functionally with Operations, Engineering, Regulatory
Affairs, and Service teams.
The Quality Manager will serve as the primary owner of the company's quality system governance, ensuring that
processes, records, and corrective actions are maintained in a state of continuous compliance and audit readiness.
This role is critical to maintaining the company's regulatory credibility, audit readiness, and quality system
integrity as SoftWave scales. The position ensures the company maintains a strong compliance backbone while enabling growth and operational execution.
Responsibilities:
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Quality Management System (QMS) Ownership
  • Own and maintain the company's QMS in alignment with applicable medical device standards
  • Develop, implement, and maintain procedures, SOPs, work instructions, and quality records
  • Manage document control, revision control, and training documentation processes
  • Ensure continuous audit readiness across all quality system elements
CAPA Ownership
  • Lead the Corrective and Preventive Action (CAPA) system
  • Ensure timely initiation, investigation, root cause analysis, and closure of CAPAs
  • Verify effectiveness of corrective actions
  • Drive cross-functional accountability for issue resolution and process improvement
Supplier Quality Oversight
  • Lead supplier qualification and quality oversight activities
  • Establish supplier quality agreements and quality performance metrics
  • Manage supplier corrective action requests (SCARs)
  • Conduct supplier quality reviews and support supplier audits
  • Partner with Supply Chain and Operations on supplier performance and issue resolution
Audit Leadership
  • Lead internal audit planning and execution
  • Serve as primary quality lead for external audits, customer audits, and certification audits
  • Coordinate responses to audit findings and corrective actions
  • Maintain audit schedules, records, and follow-up activities

Regulatory; Compliance Support
  • Support Regulatory Affairs with submission documentation and compliance records
  • Maintain quality documentation required for FDA and ISO compliance
  • Support inspection readiness and regulatory audit responses
  • Ensure quality system documentation supports product lifecycle and change control activities
    Change Control; Quality Records
  • Manage engineering change control and quality record processes
  • Ensure traceability of revisions, approvals, and controlled documentation
  • Support design transfer and sustaining engineering changes from a quality systems perspective
Performance Accountability - This role is accountable for:
  • QMS compliance status
  • CAPA cycle time and effectiveness
  • supplier quality performance
  • audit readiness and audit outcomes
  • documentation accuracy and traceability
  • quality system process compliance
Cross-Functional Interfaces - The Quality Manager will work closely with:
  • VP Operations
  • Director of Technical Operations
  • Regulatory Affairs
  • Engineering
  • Supply Chain / Procurement
  • Service Operations

Qualifications:
Required:
Education
  • Bachelor's degree in Engineering, Life Sciences, Quality, Operations, or a related technical field
  • Equivalent relevant experience may be considered in lieu of degree
  • Advanced degree is a plus, but not typically required
Experience
  • 7+ years of progressive quality experience in a regulated manufacturing environment
  • 3+ years in medical device, diagnostics, or other highly regulated industry strongly preferred
  • Prior experience owning or administering a Quality Management System (QMS)
  • Demonstrated experience with CAPA, audits, supplier quality, and document control
  • Experience supporting FDA inspections and ISO 13485 certification audits
  • Prior startup or early-stage company experience strongly preferred
Technical / Functional Qualifications
Strong working knowledge of:o ISO 13485o 21 CFR Part 820 / FDA QMSR
o CAPA systems
o document control
o training records
o change control
o supplier quality systems
o audit management
Experience leading:
o internal audits
o external audits
o supplier audits
o corrective action programs
Experience with:
o supplier qualification and SCARs
o nonconformance and deviation management
o root cause analysis
o effectiveness checks
Preferred:
  • Experience with electromechanical medical devices or capital equipment
  • Familiarity with risk management / ISO 14971
  • Working knowledge of design controls
  • Experience partnering with Regulatory Affairs on submissions and inspections
  • Experience implementing or improving electronic QMS systems (eQMS)
Physical Requirements:
• Sitting, standing and walking, which may be for extended periods of time
• Lifting and carrying, up to 100 lbs
• Pushing, pulling, and reaching overhead
• Manipulation of objects and materials, including holding, grasping, turning, and touching
• Driving
• Stooping, crouching, kneeling
• Climbing ladders or stairs
• Hearing, in-person and through the telephone or electronic device (such as a computer)
• Speaking, in-person and through the telephone or electronic device (such as a tablet or computer)
• Visual acuity, both near (i.e. clarity of vision of approximately 20 inches or less) and far (i.e. clarity of
vision of approximately 20 feet or more)
• Regular and predictable attendance
The responsibilities outlined in this job description are intended to describe the general nature and level of work
performed by individuals assigned to this role. They are not intended to be an exhaustive list of all responsibilities,
duties, and skills required. Management reserves the right to amend and change responsibilities to meet
organizational needs as necessary.
SoftWave TRT is an equal opportunity employer. We make employment decisions solely based on business needs,
job requirements, and individual qualifications without regard to race, gender, religion, ethnicity, age, or any other

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