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Senior Quality Control Engineer Jobs in Georgia (NOW HIRING)

Senior Quality Engineer

Norcross, GA · On-site

$83K - $112K/yr

This Sr. Quality Assurance Engineer will have a strong Quality background and must be able to work ... control measures, and document a robust and living risk management file. * Review and provide ...

Senior Quality Engineer

Norcross, GA · On-site

$83K - $112K/yr

This Sr. Quality Assurance Engineer will have a strong Quality background and must be able to work ... control measures, and document a robust and living risk management file. * Review and provide ...

Senior Quality Engineer

Norcross, GA · On-site

$83K - $112K/yr

This Sr. Quality Assurance Engineer will have a strong Quality background and must be able to work ... control measures, and document a robust and living risk management file. * Review and provide ...

Senior Quality Engineer

Atlanta, GA · On-site

$140K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Join Our Team as a Senior Quality Engineer Company: Coreforce Location: Atlanta (Hybrid) Job Type: Full-time Salary: Based on Experience Company Overview: Coreforce is an innovative technology ...

Senior Quality Engineer

Atlanta, GA · Hybrid

$85K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Join Our Team as a Senior Quality Engineer Company: Coreforce Location: Atlanta (Hybrid) Job Type: Full-time Salary: Based on Experience Company Overview: Coreforce is an innovative technology ...

Senior Quality Engineer

Atlanta, GA

$78K - $156K/yr

  • Medical

  • Retirement

Senior Quality Engineer The Opportunity This position works out of our Atlanta, GA location in the Heart Failure Division. In Abbott's Heart Failure (HF) business, we're developing solutions to ...

Senior Quality Engineer

Atlanta, GA · On-site

$78K - $156K/yr

  • Medical

  • Retirement

Senior Quality Engineer The Opportunity This position works out of our Atlanta, GA location in the Heart Failure Division. In Abbott's Heart Failure (HF) business, we're developing solutions to ...

Senior Quality Engineer

Atlanta, GA

$78K - $156K/yr

  • Medical

  • Retirement

Senior Quality Engineer The Opportunity This position works out of our Atlanta, GA location in the Heart Failure Division. In Abbott's Heart Failure (HF) business, we're developing solutions to ...

Sr. Quality Engineer- NPI

Duluth, GA

$81K - $110K/yr

The Senior Quality Engineer NPI (New Product Introduction) will play a critical role in ensuring ... Champion and participate in the running and creation of DFMEA/PFMEA/Control Plan activities to ...

DPR Construction is seeking a project engineer with 2+ years of quality assurance/quality control commercial construction experience. The project engineer will work on commercial projects within our ...

Senior Quality Engineer

Austell, GA · On-site

$79K - $107K/yr

ASP Global is focused on delivering high-quality software solutions, and they are seeking a Senior Quality Engineer to lead quality engineering initiatives. This role involves collaborating with ...

Control Engineer 3

Atlanta, GA · On-site

$80K - $103K/yr

Perform QA/QC and technical reviews of designs * Plans and Designs Procedures and Fixtures for ... Assists senior engineers in preparation of Bids and Proposals cost estimates and supporting ...

Control Engineer 2

Columbus, GA · On-site

$73K - $95K/yr

Perform QA/QC and technical reviews of designs * Plans and Designs * Procedures and Fixtures for ... Assists senior engineers in preparation of Bids and Proposals cost estimates and supporting ...

Senior Quality Engineer

Atlanta, GA · On-site

$85K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Senior Quality Engineer Category: Testing/Quality Assurance Main location: United States, Georgia, Atlanta Position ID:J0826-0112 Employment Type: Full Time Position Description: We are seeking a ...

Quality Engineer

Dalton, GA

$58K - $75K/yr

... Senior Quality Engineer for incoming inspections, product line patrol, outgoing quality control, and updating factory internal quality rules all in accordance with the high industry standards and ...

Quality Engineer

Dalton, GA · On-site

$63K - $82K/yr

... Senior Quality Engineer for incoming inspections, product line patrol, outgoing quality control, and updating factory internal quality rules all in accordance with the high industry standards and ...

Senior Quality Engineer

Atlanta, GA · On-site

$85K - $115K/yr

They are seeking a Senior Quality Engineer to lead the design and implementation of testing strategies and frameworks for complex systems, while mentoring junior engineers and collaborating with ...

Showing results 21-40

Senior Quality Control Engineer information

See Georgia salary details

$51.1K

$88.9K

$123.7K

How much do senior quality control engineer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for senior quality control engineer in Georgia is $88,907.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,700.00 and $101,300.00 per year, depending on experience, location, and employer.

What does a senior quality control engineer do?

A Senior Quality Control Engineer is responsible for overseeing and improving the quality assurance processes in manufacturing or production environments. They develop and implement testing methods, analyze quality data, and ensure products meet established standards and regulations. Additionally, they often lead teams, train junior staff, and collaborate with other departments to resolve quality issues and drive continuous improvement. Their expertise helps minimize defects, reduce costs, and maintain customer satisfaction.

What are some common challenges faced by senior quality control engineers in ensuring consistent product quality across multiple production lines?

Senior Quality Control Engineers often encounter challenges such as maintaining uniform quality standards across different production shifts or facilities, managing tight production schedules without compromising on thorough inspections, and adapting to rapid changes in manufacturing processes or technology. To overcome these, they typically implement robust quality management systems, conduct regular training sessions for staff, and utilize data-driven approaches to quickly identify and address variations or defects. Collaboration with cross-functional teams, such as production, R&D, and supply chain, is also crucial to proactively resolve issues and drive continuous improvement.

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

A Senior Quality Control Engineer typically requires a strong background in engineering, quality assurance methodologies, and a bachelor’s degree in a related field, often supplemented by experience in manufacturing or production environments. Familiarity with ISO standards, Six Sigma tools, statistical analysis software, and quality management systems (QMS) is highly valued. Exceptional problem-solving, attention to detail, leadership, and communication skills help drive process improvements and mentor junior staff. These competencies are crucial for ensuring consistent product quality, regulatory compliance, and efficiency within complex production settings.

What is the difference between Senior Quality Control Engineer vs Quality Control Technician?

AspectSenior Quality Control EngineerQuality Control Technician
CredentialsBachelor's degree in engineering or related field, often with certifications like CQEHigh school diploma or associate degree, technical training
Work EnvironmentDesigning quality systems, analyzing data, overseeing testing processesPerforming routine inspections, testing products, recording results
Employer & Industry UsageManufacturing, aerospace, automotive, pharmaceuticalsManufacturing plants, production lines, quality assurance labs
Common Search & ComparisonSenior Quality Control Engineer vs Quality Control Technician

The main difference between a Senior Quality Control Engineer and a Quality Control Technician lies in their responsibilities and qualifications. The engineer typically handles complex analysis, system development, and oversight, requiring higher education and certifications. The technician focuses on routine testing and inspections. Both roles are essential in manufacturing and quality assurance environments, but they differ in scope and expertise.

What are the most commonly searched types of Quality Control Engineer jobs in Georgia?

The most popular types of Quality Control Engineer jobs in Georgia are:

What cities in Georgia are hiring for Senior Quality Control Engineer jobs?

Cities in Georgia with the most Senior Quality Control Engineer job openings:

Infographic showing various Senior Quality Control Engineer job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $88,907 per year, or $42.7 per hour.

Senior Quality Engineer

Werfen

Norcross, GA • On-site

$83K - $112K/yr

Full-time

Re-posted 12 days ago


Werfen rating

8.7

Company rating: 8.7 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Introduction
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care
Overview
Werfen
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
This is a hands-on role where the Sr. Quality Assurance Engineer will apply diversified knowledge of engineering, quality principles and practices for medical device products and in vitro diagnostic devices (EU and FDA).This individual will ensure that all system-level projects deliverables (e.g., plans, requirements, specifications, tests, test results, traceability, risk management documents, reports) meet quality and compliance requirements. This Sr. Quality Assurance Engineer will have a strong Quality background and must be able to work in a team environment and be able to communicate clearly across all disciplines including Research & Development, Regulatory Affairs, Post Market Surveillance, Manufacturing Operations, Marketing, Validation, Manufacturing Technical Support and Regulatory Agencies. If you have the required skills, don't wait, apply today!!
This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time .
Responsibilities
Key Accountabilities:
  • Lead risk management initiatives for the entire product lifecycle in accordance with ISO14971 and related regulatory requirements. Assure applicable quality decisions are derived from the appropriate risk management document in accordance to the quality system.
  • Independently manage and facilitate new risk assessments from initiation to completion working cross-functionally to develop risk management plans with key stakeholders that are robust and compliant with all procedural and regulatory requirements.
  • Collaborate at a systems level with R&D, Clinical, and other key functions to identify risks, implement risk control measures, and document a robust and living risk management file.
  • Review and provide feedback for changes to designs and processes and assess their impact to assure risk management requirements are met.
  • Support on-going product compliance technical documentation and on-going market authorizations through review and response to competent authority feedback in a timely manner.
  • Support teams to establish product development requirements e.g., Design Input Document, Design Verification and Validation requirements, Risk Management requirements, Usability requirements, CTQ Identification etc.
  • Support DHF content completion, collaboratively communicating and resolving regulatory compliance gaps.
  • Serve as a Quality Core Team member on sustaining product lifecycle project and new product development teams. Represent Quality for new and existing product improvement, manufacturing transfers, and quality plan initiatives.
  • Assist in the QA review and approval of process and equipment validation / qualifications (IQ, OQ, PQ).
  • Assist in QA review and approval of software user acceptance testing.

Qualifications
Minimum Knowledge & Experience required for the position:
  • Minimum of 5 years medical device experience in Quality or R&D Engineering position with risk management, design control and product development experience.
  • Experience in the IVD industry, preferred.
  • Bachelor's degree (BA/BS) from a four-year college or university; or equivalent combination of education and experience.
  • BS in Engineering or associated scientific discipline, preferred
  • Quality certification, such as CQE (Certified Quality Engineer) or CQA (Certified Quality Auditor), or ASQ, and/or SSBB, preferred
  • Proficient in Microsoft Word, Excel, and managing electronic data files.
  • Extensive hands-on experience with the ISO 14971 standard with demonstrated experience in implementing a device risk management process based on the standard and/or executing a RM.

Additional requirements:
  • Strong working knowledge of risk management, CAPA, and Design Controls.
  • Some experience in systems engineering and/or device development including connected systems and software as a medical device (SaMD)

Closing
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.
www.werfen.com

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About Werfen

Sourced by ZipRecruiter

Industry

Health care and social assistance

Company size

1,001 - 5,000 Employees

Headquarters location

L'Hospitalet de Llobregat, Barcelona, ES