ZipRecruiter

Log In

1

Medical Device Manufacturing Jobs in Georgia (NOW HIRING)

CorDx

Quality Assurance Manager

Chamblee, GA · On-site

... medical device manufacturing . * 3+ years in a managerial or leadership role overseeing QA teams. * Skills & Competencies * Strong knowledge of US FDA, ISO 13485, and other regulatory standards

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

... medical device manufacturing . * 3+ years in a managerial or leadership role overseeing QA teams. * Skills & Competencies * Strong knowledge of US FDA, ISO 13485, and other regulatory standards

CorDx

Quality Assurance Manager

Alpharetta, GA

... medical device manufacturing . * 3+ years in a managerial or leadership role overseeing QA teams. * Skills & Competencies * Strong knowledge of US FDA, ISO 13485, and other regulatory standards

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

... medical device manufacturing . * 3+ years in a managerial or leadership role overseeing QA teams. * Skills & Competencies * Strong knowledge of US FDA, ISO 13485, and other regulatory standards

Chemence

Facilities Engineer

Alpharetta, GA · On-site

Must have 4 years of experience in a facilities engineering role working in a medical device manufacturing environment. * Must include experience working within cGMP, ISO and FDA regulations ...

CorDx

Quality Assurance Manager

Chamblee, GA

... medical device manufacturing . * 3+ years in a managerial or leadership role overseeing QA teams. * Skills & Competencies * Strong knowledge of US FDA, ISO 13485, and other regulatory standards

CorDx

Quality Manager

Atlanta, GA · On-site

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 ...

CorDx

Quality Manager

Atlanta, GA · On-site

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 ...

CorDx

Quality Manager

Atlanta, GA · On-site

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 ...

Cordx Inc

Senior Operations Manager

Alpharetta, GA · On-site

Experience: 10+ years in biotech, diagnostics, or medical device manufacturing, with 5+ years in leadership roles managing cross-functional operations teams. * Strong track record of role stability ...

CorDx

Supply Chain Manager

Atlanta, GA · On-site

$80K - $120K/yr

Proven experience in supply chain management, ideally within pharma, biotech, or medical device manufacturing. Technical & Operational Skills: * Strong knowledge of supply chain processes, logistics ...

previous pagenext page

Showing results 21-40

All JobsMedical Device Manufacturing JobsMedical Device Manufacturing Jobs in Georgia

Medical Device Manufacturing information

See Georgia salary details

$15

$22

$33

How much do medical device manufacturing jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for medical device manufacturing in Georgia is $22.90, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $26.78 per hour, depending on experience, location, and employer.

What is a medical device manufacturing job?

A Medical Device Manufacturing job involves producing, assembling, and testing medical devices to ensure they meet regulatory and quality standards. Workers in this field may operate machinery, inspect products, and follow strict guidelines to maintain safety and efficiency. Roles can range from machine operators and quality control inspectors to engineers and regulatory compliance specialists. This industry is essential for creating devices like surgical instruments, pacemakers, and diagnostic equipment used in healthcare. Attention to detail, adherence to regulations, and technical skills are key for success in this field.

What are the key skills and qualifications needed to thrive in medical device manufacturing?

To thrive in Medical Device Manufacturing, you need strong attention to detail, knowledge of quality assurance processes, and an understanding of regulatory standards such as ISO 13485 or FDA requirements. Experience with manufacturing equipment, ERP systems, and specialized tools for assembly and testing is typically required, and certification in areas like Six Sigma or Lean Manufacturing can be advantageous. Effective communication, teamwork, and problem-solving skills help individuals excel in fast-paced, multidisciplinary environments. These skills are vital for maintaining product safety, ensuring regulatory compliance, and meeting production targets in the highly regulated medical device industry.

What career advancement opportunities are available in medical device manufacturing?

Medical Device Manufacturing offers a variety of career advancement paths, allowing employees to move into roles such as production supervisor, quality assurance specialist, or process engineer as they gain experience. Many companies provide on-the-job training, mentorship programs, and support for additional certifications to help employees further develop their technical and leadership skills. Team members who demonstrate strong performance and a commitment to continuous improvement may also transition into management positions or cross-functional roles in research and development, regulatory affairs, or supply chain management. This field values both specialized technical expertise and a proactive approach to professional growth, providing long-term career stability and diverse opportunities.

Is medical device manufacturing a good career?

Medical device manufacturing is a stable career that involves assembling, testing, and quality control of medical equipment, often requiring technical skills and certifications. It offers opportunities for advancement and typically provides a clean, regulated work environment, with demand driven by healthcare industry growth.

What are popular job titles related to Medical Device Manufacturing jobs in Georgia?

For Medical Device Manufacturing jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Medical Device Manufacturing jobs in Georgia look for?

The top searched job categories for Medical Device Manufacturing jobs in Georgia are:

What cities in Georgia are hiring for Medical Device Manufacturing jobs?

Cities in Georgia with the most Medical Device Manufacturing job openings:

Medical Device Manufacturing jobs near you
Infographic showing various Medical Device Manufacturing job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $47,633 per year, or $22.9 per hour.

Quality Assurance Manager

CorDx

Chamblee, GA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 10 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.  
Position: QA Manager
Location: Alpharetta/Chamblee
Position Type: 5 days Onsite Exempt Position

Job Summary: We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the development, manufacturing, and distribution of Class II IVD devices. The ideal candidate will have at least 7 years of experience in the IVD industry, with a strong background in quality management systems, regulatory compliance, and team leadership.

Key Responsibilities:

Quality Systems & Compliance

  • Develop, implement, and maintain Quality Management Systems (QMS) in accordance with, US FDA, ISO 13485, and applicable regulations.
  • Lead internal and external audits, regulatory inspections, and corrective action plans (CAPAs).
  • Oversee batch record reviews, deviations, non-conformance reports (NCRs), and change controls to maintain product quality and integrity.

Process & Product Quality Assurance

  • Develop and enforce Standard Operating Procedures (SOPs) and best practices to ensure consistent quality across manufacturing operations.
  • Collaborate with R&D, production, and regulatory affairs teams to ensure new products and processes meet quality standards.
  • Monitor and analyze quality metrics (KPIs) to drive continuous improvement initiatives.
  • Ensure adherence to Good Documentation Practices (GDP) and data integrity policies.

Leadership & Team Development

  • Lead, mentor, and develop the QA team, fostering a culture of quality, compliance, and continuous improvement.
  • Train manufacturing and quality teams on quality systems, and root cause analysis (RCA) methodologies.
  • Serve as the primary point of contact for quality-related issues and escalations.

Risk Management & Continuous Improvement

  • Identify quality risks and implement proactive mitigation strategies.
  • Lead investigations and root cause analyses for product defects, deviations, and non-conformances.
  • Drive LEAN, Six Sigma, or other process improvement initiatives to enhance efficiency and reduce waste.
  • Stay updated on industry trends, new regulations, and technological advancements in medical device IVD quality assurance.

Requirements

  • Bachelor’s or Master’s degree in Biotechnology, Microbiology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
  •   7+ years of experience in quality assurance within biotech, pharmaceutical, or medical device manufacturing.
  •  3+ years in a managerial or leadership role overseeing QA teams.
  • Skills & Competencies
  • Strong knowledge of US FDA, ISO 13485, and other regulatory standards.
  • Experience with QA audits, inspections, CAPA investigations, and risk management.
  • Proficiency in QMS software and documentation control systems.
  • Strong analytical and problem-solving skills, with a data-driven approach to decision-making.
  • Excellent leadership, communication, and cross-functional collaboration skills.

Benefits

  • Medical Insurance Plan
  • Retirement Plan
  • 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.