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Quality Associate Jobs in Athens, GA (NOW HIRING)

Quality Control Microbiology Lab Supervisor

Athens, GA · On-site

$24.50 - $32.25/hr

A minimum of an associate degree and/or bachelor's degree in microbiology or a related science field is preferred. Required: * A minimum of 2 years of experience in a QC Microbiology lab within the ...

Conduct internal quality investigations and resolve issues related to non-conforming parts on axle drive assembly lines. * Plan, test, train, supervise, and implement preventive quality assurance ...

Warehouse Associate

Braselton, GA · On-site

$17.50/hr

Must have at least 6 months of Quality Inspecting or Baling experience to be considered for the ... Associates may be required to stay longer until work is complete (flexibility required) - Weekends ...

Warehouse Associate

Braselton, GA · On-site

$14.50 - $17.25/hr

About the job Warehouse Associate We are looking for Warehouse Associates for a client in the North ... Perform inventory controls and keep quality standards high for audits * Keep a clean and safe ...

Warehouse Associate

Braselton, GA · On-site

$17.50/hr

Must have at least 6 months of Quality Inspecting or Baling experience to be considered for the ... Associates may be required to stay longer until work is complete (flexibility required) -Weekends ...

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Quality Associate information

See Athens, GA salary details

$10

$26

$48

How much do quality associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for quality associate in Athens, GA is $26.00, according to ZipRecruiter salary data. Most workers in this role earn between $17.64 and $30.38 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 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 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 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 most commonly searched types of Quality jobs in Athens, GA?

The most popular types of Quality jobs in Athens, GA are:

What are popular job titles related to Quality Associate jobs in Athens, GA?

For Quality Associate jobs in Athens, GA, the most frequently searched job titles are:

What job categories do people searching Quality Associate jobs in Athens, GA look for?

The top searched job categories for Quality Associate jobs in Athens, GA are:

What cities near Athens, GA are hiring for Quality Associate jobs?

Cities near Athens, GA with the most Quality Associate job openings:

Infographic showing various Quality Associate job openings in Athens, GA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $54,090 per year, or $26 per hour.

Quality Control Microbiology Lab Supervisor

Johnson and Johnson

Athens, GA • On-site

$24.50 - $32.25/hr

Full-time

Posted 9 days ago


Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
People Leader
All Job Posting Locations:
Athens, Georgia, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Quality Control Microbiology Lab Supervisor to be located in Athens, GA.
The Microbiology Lab Supervisor is responsible for the safety, organization, administration and supervision of the Lab Analysts. Leading, mentoring, and developing a high-performing team to ensure the timely and accurate testing of raw materials, in-process samples, and finished goods in accordance with internal and compendia specifications.
This role balances technical microbiological expertise with strong people leadership to ensure laboratory compliance (GMP/GLP) while promoting a culture of safety, continuous improvement, and employee engagement. Assures compliance with all quality control policies, procedures and systems to ensure the timely release of high-quality products in support of the supply chain process.
You will be responsible for:
  • Mentors and supervises quality control employees, evaluates performance, and conveys goals effectively to enhance product quality and customer satisfaction.
  • Provides technical and regulatory guidance related to lab operations and seeks continuous process improvements in cost, quality, and compliance.
  • Review/approve test data, technical reports and standard operating procedures.
  • Assures all laboratory responsibilities are performed in accordance with internal and external regulations and policies and consistent with supply chain cycle time goals.
  • Adhering to all state and federal regulations, including FDA, EPA, OSHA, and DEA guidelines, as well as following company and site-specific policies and procedures.
  • Participates in global initiatives, performs gap assessments, and provides input for quality control reports, budget planning, and project leadership on method transfers, validations, and equipment purchases.
  • Upholds the Johnson & Johnson Credo, promoting safety and personal development while ensuring regulatory compliance of laboratory operations.
  • Serves as an SME or in a support role for inspections and audits.
  • Contributing insights to address intricate investigations, focusing on identifying the root cause and implementing effective corrective and preventive measures, all while ensuring the prompt resolution of laboratory inquiries.

Qualifications
Education:
  • A minimum of an associate degree and/or bachelor's degree in microbiology or a related science field is preferred.

Required:
  • A minimum of 2 years of experience in a QC Microbiology lab within the pharmaceutical industry or relevant military experience.
  • A minimum of 2 years of experience in a supervisory or team lead role, with demonstrated ability to develop staff. Excellent communication and conflict handling skills.

Preferred:
  • Strong working knowledge of FDA regulations, USP standards, GMP/GLP requirements and Contamination Control Strategy Programs.
  • Experience in aseptic techniques.
  • Ability to inspire and motivate associates, fostering a collaborative project team environment.
  • Highly detail-oriented with excellent communication, organizational, investigative, and negotiation/influencing skills.
  • Must possess the capability to make crucial decisions for effectively managing laboratory teams while recognizing and discussing interdependencies and impacts with upper management.
  • Decisions and problem-solving in this role must align with higher-level organizational and business needs, ensuring full consideration of regulatory requirements, sound business practices, and scientific validity.
  • Must demonstrate strong organizational agility, enabling rapid and effective responses to dynamic business needs.

Other:
  • This position may require availability for working multiple shifts, including irregular (non-standard) shifts and/or weekends.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.
#LI-Onsite
Required Skills:
Preferred Skills:
Collaboration, Compliance Management, Controls Compliance, Corrective and Preventive Action (CAPA), Developing Others, Inclusive Leadership, ISO 9001, Leadership, Operational Excellence, Persistence and Tenacity, Quality Auditing, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Report Writing, Technologically Savvy