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Quality Manager Medical Device Jobs in Georgia (NOW HIRING)

Quality Manager Location: Onsite - Atlanta Office We are seeking an experienced Quality Manager to ... The ideal candidate will have a minimum of 10 years of relevant experience in the medical device ...

Quality Manager Location: Onsite - Atlanta Office We are seeking an experienced Quality Manager to ... The ideal candidate will have a minimum of 10 years of relevant experience in the medical device ...

Quality Manager Location: Onsite - Atlanta Office We are seeking an experienced Quality Manager to ... The ideal candidate will have a minimum of 10 years of relevant experience in the medical device ...

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 ...

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This role is responsible for developing new business, managing existing accounts, and serving as a ... Innovative, high-quality medical products that improve patient outcomes * Supportive and ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

... Medical Device industries. We understand the clinical trial process from Phase I through Phase IV. ... Supplier Quality Manager Detailed Coordinate completion of Specification Agreements with suppliers.

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Quality Manager Medical Device information

See Georgia salary details

$20.3K

$72.8K

$133.4K

How much do quality manager medical device jobs pay per year?

As of Aug 30, 2026, the average yearly pay for quality manager medical device in Georgia is $72,751.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,200.00 and $114,800.00 per year, depending on experience, location, and employer.

What does a quality manager do in the medical device industry?

A Quality Manager in the medical device industry is responsible for ensuring that products meet all regulatory requirements and quality standards throughout their lifecycle. They develop, implement, and monitor quality management systems, oversee internal and external audits, and work closely with manufacturing, engineering, and regulatory teams to maintain compliance with standards such as ISO 13485 and FDA regulations. Their role is critical to ensuring patient safety and product efficacy by preventing defects and ensuring consistent quality.

What are the key skills and qualifications needed to thrive as a quality manager in the medical device industry?

To thrive as a Quality Manager in the Medical Device industry, you need a solid background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and process improvement, often supported by a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), risk management tools (like FMEA), and certifications such as ASQ Certified Quality Auditor (CQA) or Six Sigma are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring cross-functional alignment. These skills and qualifications are crucial to ensure product safety, regulatory compliance, and the overall success of medical device manufacturing and delivery.

What are some common challenges quality managers face when ensuring compliance in the medical device industry?

Quality Managers in the medical device industry often encounter challenges such as keeping up with evolving regulatory requirements (like FDA, ISO 13485, and MDR), coordinating cross-functional teams to maintain strict quality standards, and managing documentation for audits. They must also address nonconformities quickly and implement corrective and preventive actions to avoid product recalls. Effective communication and strong attention to detail are essential for navigating these challenges while maintaining product safety and regulatory compliance.

What is the difference between Quality Manager Medical Device vs Quality Engineer Medical Device?

AspectQuality Manager Medical DeviceQuality Engineer Medical Device
Primary FocusOversees quality systems, compliance, and team managementDesigns, develops, and implements quality testing and inspection processes
CertificationsISO 13485, Six Sigma, Lead AuditorISO 13485, Six Sigma, Certified Quality Engineer (CQE)
Work EnvironmentManagement, regulatory compliance, cross-department collaborationProduct testing, process improvement, technical analysis
Industry UsageUsed across organizations to ensure overall quality managementUsed in product development and testing phases

The main difference is that the Quality Manager Medical Device focuses on managing quality systems and compliance at a strategic level, while the Quality Engineer Medical Device concentrates on technical testing and process improvements. Both roles require similar certifications and work within the same industry but serve different functions within quality assurance.

What cities in Georgia are hiring for Quality Manager Medical Device jobs?

Cities in Georgia with the most Quality Manager Medical Device job openings:

Infographic showing various Quality Manager Medical Device job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 15% Part Time, 11% Contract, and 3% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $72,751 per year, or $35 per hour.

Quality Manager

CorDx

Atlanta, GA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 29 days ago


Job description

Who is CorDx?
CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.
Job Type: Full time
Job Title: Quality Manager
Location: Onsite - Atlanta Office
We are seeking an experienced Quality Manager to join our team in the IVD (In Vitro Diagnostic) industry. The ideal candidate will have a minimum of 10 years of relevant experience in the medical device manufacturing sector, with a strong background in quality management systems, regulatory compliance, and ISO standards. The Quality Manager will play a critical role in implementing, managing, and improving our company's quality management system, with a focus on IVD products and equipment.
Key Responsibilities:
  1. Implement, manage, and improve the company's quality management system, with a primary focus on IVD products and equipment.
  2. Conduct internal audits, compile audit reports, perform problem analysis, propose improvement initiatives, and monitor the implementation of corrective and preventive actions (CAPA).
  3. Lead and participate in internal audits and management reviews of the company's quality system as a key member of the quality department.
  4. Manage the documentation of the company's quality management system, ensuring compliance with relevant standards and regulations.
  5. Oversee the quality management system for IVD equipment, ensuring compliance with applicable regulations and standards.
  6. Perform statistical analysis of IVD equipment quality data, prepare reports, and develop corrective and preventive measures as needed.
  7. Update company documents in accordance with new or revised quality standards, laws, and regulations.
  8. Establish collaborative relationships with key opinion leaders and certification bodies to ensure alignment with industry best practices and regulatory requirements.

Requirements
  1. Minimum Bachelor's degree in Science or related field.
  2. ISO 13485:2016 lead auditor certification preferred.
  3. Thorough knowledge of US FDA 21 CFR 820 Quality System Regulation and ISO 13485:2016 standards.
  4. Strong understanding of quality management principles and practices in the medical device industry.
  5. Excellent communication and interpersonal skills.
  6. Ability to work collaboratively in a team environment.
  7. Demonstrated problem-solving and analytical skills.
  8. Attention to detail and strong organizational skills.
  9. Minimum 10 Years experience in Medical devices, Quality Management , Regulatory compliance and ISO standards

Benefits
  • Health Care Plan (Medical)
  • 401K
  • Paid Time Off
  • Training & Development

We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.