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Quality Oversight Engineer Jobs in Georgia (NOW HIRING)

SoftWave TRT

Quality Manager

Marietta, GA · On-site

... oversight, CAPA administration, audit readiness, and regulatory support activities, while working cross-functionally with Operations, Engineering, Regulatory Affairs, and Service teams. The Quality ...

4pconsultinginc

Quality Coordinator 3

Lakemont, GA · On-site

CWI/AWS certification and 10+ years of quality oversight experience (or a 4-year degree in a ... Demonstrated ability to collaborate with contractors, engineers, and project managers

4pconsultinginc

Quality Lead 2

Columbus, GA · On-site

Key Responsibilities * Quality Planning & Oversight * Assist project management with the ... Review and redline engineering drawings, specifications, and submittals to ensure compliance.

SMI Composites

Quality Engineer

Comer, GA · On-site

$65K - $75K/yr

Quality Assurance Oversight * Monitor compliance with control plans, process sheets, inspection ... Bachelor's Degree in Engineering, preferably Mechanical, Industrial, Materials, or equivalent ...

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Quality Oversight Engineer information

What is a quality oversight engineer?

Quality Oversight Engineers are professionals responsible for ensuring that products, processes, and systems meet established quality standards and regulatory requirements. They monitor manufacturing or production operations, conduct audits, and collaborate with various teams to identify and resolve quality issues. Their role often includes reviewing documentation, implementing corrective actions, and ensuring compliance with industry regulations to maintain high-quality outputs. Additionally, they may provide training and guidance to staff on quality best practices and assist in continuous improvement initiatives.

How does a quality oversight engineer typically collaborate with cross-functional teams to ensure compliance and product quality?

Quality Oversight Engineers work closely with production, engineering, and regulatory teams to monitor processes and ensure adherence to quality standards. They often participate in project meetings, conduct audits, and review documentation to identify potential risks or non-conformities. Effective communication and teamwork are essential, as these engineers provide feedback, recommend corrective actions, and help implement process improvements. This collaborative environment helps maintain high product quality and regulatory compliance throughout the manufacturing lifecycle.

What are the key skills and qualifications needed to thrive as a quality oversight engineer, and why are they important?

To thrive as a Quality Oversight Engineer, you need a solid background in quality management, engineering principles, and regulatory compliance, often supported by a degree in engineering or a related field. Familiarity with quality management systems (QMS), ISO standards, root cause analysis tools, and certifications such as Six Sigma or ASQ CQE are common requirements. Strong attention to detail, problem-solving abilities, and effective communication are vital soft skills to excel in this role. These competencies ensure that products and processes consistently meet standards, mitigate risks, and support organizational excellence.

What is the difference between Quality Oversight Engineer vs Quality Assurance Engineer?

AspectQuality Oversight EngineerQuality Assurance Engineer
CertificationsISO, Six Sigma, ASQ certifications often preferredISO, Six Sigma, ASQ certifications often preferred
Work EnvironmentRegulated industries like pharmaceuticals, medical devices, manufacturingSoftware, manufacturing, service industries
Primary FocusOverseeing compliance, audits, and quality systemsDeveloping and executing testing plans, process improvements
Employer UsageManufacturers, biotech, pharma companiesTech companies, manufacturing, software firms

While both roles focus on quality, the Quality Oversight Engineer primarily ensures compliance and oversees quality systems, often in regulated industries. The Quality Assurance Engineer concentrates on testing, process improvements, and preventing defects during product development. Understanding these differences helps candidates target the right roles based on their skills and industry focus.

Are quality oversight engineers paid well?

Quality oversight engineers typically earn competitive salaries that reflect their expertise in quality assurance, compliance, and process improvement. Compensation varies based on experience, industry, and location, but they generally receive benefits and opportunities for advancement in manufacturing, aerospace, or healthcare sectors.

Is a Quality Oversight Engineer a good career?

A Quality Oversight Engineer is a valuable role focused on ensuring product and process quality through inspections, audits, and compliance with standards. It often requires knowledge of quality management systems, industry regulations, and relevant certifications, making it a stable career with opportunities for advancement in manufacturing, healthcare, or technology sectors.

What are popular job titles related to Quality Oversight Engineer jobs in Georgia?

For Quality Oversight Engineer jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Quality Oversight Engineer jobs in Georgia look for?

The top searched job categories for Quality Oversight Engineer jobs in Georgia are:

What cities in Georgia are hiring for Quality Oversight Engineer jobs?

Cities in Georgia with the most Quality Oversight Engineer job openings:

Quality Oversight Engineer jobs near you
Infographic showing various Quality Oversight Engineer job openings in Georgia as of June 2026, with employment types broken down into 1% As Needed, 85% Full Time, and 14% Part Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Quality Manager

SoftWave Tissue Regeneration Technologies

Marietta, GA • On-site

Full-time

Posted 15 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:
  • 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
  • CAPA systems
  • document control
  • training records
  • change control
  • supplier quality systems
  • audit management
Experience leading:
  • internal audits
  • external audits
  • supplier audits
  • corrective action programs

Experience with:
  • supplier qualification and SCARs
  • nonconformance and deviation management
  • root cause analysis
  • 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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