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Quality Associate Jobs in Atlanta, GA (NOW HIRING)

Regularly exercises discretion and in performing duties directly related to the general operation of product quality control. RESPONSIBILITIES Provide technical, customer relations, and personnel ...

SUMMARY The Quality Team Supervisor will lead and oversee quality assurance activities on-site to ... Associate or bachelor's degree preferred ( relevant work experience may be considered as an ...

Perform OJT training of newly hired associates. * Collaborate with teams to conduct associate ... Support Quality Supervisor, Production Supervisor, and Production Manager to meet/exceed goals.

SUMMARY The Quality Team Supervisor will lead and oversee quality assurance activities on-site to ... Associate or bachelor's degree preferred (relevant work experience may be considered as an ...

Perform OJT training of newly hired associates. * Collaborate with teams to conduct associate ... Support Quality Supervisor, Production Supervisor, and Production Manager to meet/exceed goals.

Perform OJT training of newly hired associates. * Collaborate with teams to conduct associate ... Support Quality Supervisor, Production Supervisor, and Production Manager to meet/exceed goals.

Showing results 21-40

Quality Associate information

See Atlanta, GA salary details

$10

$25

$48

How much do quality associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for quality associate in Atlanta, GA is $25.90, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $30.29 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

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

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

What are the most commonly searched types of Quality jobs in Atlanta, GA? The most popular types of Quality jobs in Atlanta, GA are:
What are popular job titles related to Quality Associate jobs in Atlanta, GA? For Quality Associate jobs in Atlanta, GA, the most frequently searched job titles are:
What cities near Atlanta, GA are hiring for Quality Associate jobs? Cities near Atlanta, GA with the most Quality Associate job openings:
Infographic showing various Quality Associate job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, 6% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $53,870 per year, or $25.9 per hour.

Sr. Quality Assurance Associate

Avion Pharmaceuticals

Alpharetta, GA • On-site

Full-time

Re-posted 29 days ago


Job description

Third Party Quality Senior Associate

Job Description
The Third Party Quality Senior Associate will be responsible for the review and disposition of batch record documentation for Alora distributed products manufactured by external third parties in accordance with site SOP and regulatory guidance. The position will also perform the quality review of related cGMP documentation for Alora distributed products, including annual product reviews, and will assist with the coordination of global change controls.

Key Responsibilities/Essential Functions

  • Critically review and disposition batch record documentation for products manufactured by external third parties.
  • Perform the quality review of related cGMP documentation generated at third parties including, but not limited to deviations, out-of-specification investigations, change controls, process validation protocols/reports, and master batch records.
  • Assign and/or approve lot numbers and expiration dates for products transferred to packaging facilities, as required.
  • Review annual product reviews generated by third party vendors. Collect, review, and report product data needed to supplement third-party vendor annual product reviews.
  • Collect and review the changes to USP and initiate any associated change controls related to those changes. Assist with the execution of a corporate USP change management system.
  • Monitor and assist with the implementation of new corporate policies.
  • Collect and review the changes to regulatory policies and assist in the implementation of these policies.
  • Review and approve product labeling.
  • Escalate issues to Quality Management, as appropriate, including, but not limited to, product quality, safety, or efficacy concerns identified in annual product reviews and critical issues identified as part of batch record review and related records.
  • Track closure of assigned Third Party Quality records.
  • Monitor due dates for submission of annual product reviews and perform follow-up activities.
  • Assist with the generation of quality system metrics and trending reports.
  • Assist with the performance of high-risk or global risk assessment impacting Alora manufactured and/or distributed products.
  • Assist with the development and maintenance of procedures that define the cGMP activities within the areas of responsibility.
  • Provide training and guidance to more junior Associates within the Third Party Quality team.
  • Champion quality improvement processes within the areas of responsibility to ensure adherence to cGMPs and foster continuous improvement.
  • Support a culture of quality and continuous improvement throughout the organization.
  • Perform additional duties and responsibilities as assigned by Quality Management.

Basic Qualifications

  • A Bachelor's degree preferred and/or 4 years of related work experience.
  • Minimum of 2 years of quality experience in FDA regulated industries (pharmaceutical or biotech industries, preferred).
  • Thorough knowledge of FDA Quality System requirements.

Other Requirements

  • Ability to work independently when guided by documented procedures.
  • Able to work effectively as part of a team.
  • Excellent attention to detail.
  • Ability to deliver within established timelines.
  • Fluency in English and excellent comprehension.
  • Strong oral and written communication skills.
  • Proficient with Microsoft office applications.