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Quality Associate Jobs (NOW HIRING)

Quality Associate Pay rate based on experience! About Codis At Codis (formerly Particle Dynamics), we manufacture high-quality pharmaceutical, nutraceutical, food, and over-the-counter products that ...

As a Quality Associate at TR Toppers, Inc., you will contribute to our commitment to maintaining superior food quality and safety. In this role, you will perform product inspections, laboratory ...

Quality Associate Department: Quality and Regulatory Location: On-site at HQ in Somerville, MA Reports to: Director, Quality and Regulatory Key Relationships: Sr. Quality Engineer, Device Operations ...

Quality Associate

Maple Grove, MN · On-site

$52K - $67K/yr

The Quality Associate issues cGMP documentation to operations in support of manufacturing and packaging operations. Reviews executed manufacturing/packaging documentation and dispositions batch ...

Quality Associate

Lebanon, OR · On-site

$22.10/hr

What You'll Do As a Quality Associate , you'll play a key role in supporting ENTEK's quality assurance processes by testing production samples, verifying raw materials, and communicating results to ...

What You'll Do As a Quality Associate , you'll play a key role in supporting ENTEK's quality assurance processes by testing production samples, verifying raw materials, and communicating results to ...

Summary The Quality Associate supports both quality assurance and quality control initiatives regarding Production and Operations to ensure that customer requirements are met, and any discrepancies ...

Quality Associate

Oakland, CA · On-site

$19 - $22/hr

A Level II Associate is always watchful for quality risks around them and takes action even when outside their normal inspection duties. The individual MAY be cross trained to work in multiple ...

Quality Associate

Florida, NY · On-site

$23/hr

Learn more about us at ABOUT THE JOB The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe ...

Quality Associate

Florida, NY · On-site

$23/hr

Learn more about us at ABOUT THE JOB The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe ...

Our Quality Department has an opening for a Quality Associate that works Monday - Friday, 9:00 AM - 5:30 PM. This position supports the continuous flow of quality test cell activities by testing and ...

Quality Associate

South Bend, IN · On-site

$15.94 - $18/hr

Our Quality Department has an opening for a Quality Associate that works Monday - Friday, 9:00 AM - 5:30 PM. This position supports the continuous flow of quality test cell activities by testing and ...

Learn more about us at ABOUT THE JOB The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe ...

We are seeking a detail-oriented and motivated Quality Associate to join our team. In this role, you will support the day-to-day operations of our Quality Assurance (QA) and facility compliance ...

We are seeking a detail-oriented and motivated Quality Associate to join our team. In this role, you will support the day-to-day operations of our Quality Assurance (QA) and facility compliance ...

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Quality Associate information

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How much do quality associate jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for quality associate in the United States is $26.93, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $31.49 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 cities are hiring for Quality Associate jobs?

Cities with the most Quality Associate job openings:

What are the most commonly searched types of Quality jobs?

The most popular types of Quality jobs are:

Who are the top companies hiring for Quality Associate jobs?

The top employers for Quality Associate jobs are:

What states have the most Quality Associate jobs?

States with the most job openings for Quality Associate jobs include:

Infographic showing various Quality Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $56,018 per year, or $26.9 per hour.

Quality Associate

Codis

Seymour, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago


Job description

Quality Associate

Pay rate based on experience!

About Codis

At Codis (formerly Particle Dynamics), we manufacture high-quality pharmaceutical, nutraceutical, food, and over-the-counter products that support better health worldwide. We're a three-shift operation with a close-knit team that values collaboration, growth, and hands-on learning.

Why You'll Love Working Here

  • Paid time off available from day one - no waiting period - 80 hours of vacation and 56 hours of sick/personal time annually
  • Competitive pay for experience and performance
  • Health, dental, vision, and life insurance effective the 1st of the month after hire
  • 401(k) match: 100% match on the first 3% contributed, and 50% match on the next 2% - with immediate vesting
  • Clean, climate-controlled pharmaceutical environment
  • Growth opportunities within a supportive and collaborative environment
  • 10 paid holidays per year, effective upon hire

Position Summary

We are currently seeking a Quality Associate to join our Seymour Quality team. This position plays a key role in ensuring that all products meet quality, safety, and regulatory standards through testing, documentation, and compliance with internal and external requirements. The Quality Associate performs all activities in accordance with Codis' Standard Operating Procedures (SOPs) and applicable regulations (FDA, EU, USP/NF, etc.).

Primary Responsibilities

  • Perform and document incoming, in-process, and finished product testing to ensure accuracy, compliance, and product integrity.
  • Conduct line checks, start-up checks, and cleaning verifications to support operations.
  • Review batch records and manufacturing documentation for completion and compliance.
  • Report any discrepancies or non-conformances immediately to management.
  • Conduct USP water sampling and testing and Environmental Monitoring per established procedures.
  • Monitor product quality through chemical and physical laboratory testing.
  • Prepare Certificates of Analysis (C of A), Certificates of Compliance (C of C), and Certificates of Testing (C of T) as needed.
  • Manage reagent inventory and ensure adequate supplies for production schedules.
  • Maintain retention samples and documentation for raw materials and finished products.
  • Administer the stability program, ensuring timely collection, testing, and reporting of stability samples.
  • Coordinate with maintenance to ensure laboratory instruments and data loggers are calibrated and compliant.
  • Monitor and document temperature control for warehouse and refrigerated storage areas.
  • Perform incoming material sampling, testing, and disposition according to procedures.
  • Maintain organized laboratory notebooks, cleanliness, and order.
  • Participate in internal audits, continuous improvement initiatives, and change control processes.
  • Assist in investigations (NOEs), write summary reports, and recommend CAPAs as needed.
  • Review compendial methods annually and initiate change control when required.
  • Perform other related duties as assigned.

Qualifications

  • Prior experience in a quality assurance or laboratory environment within pharmaceutical or related manufacturing preferred.
  • Working knowledge of GMP, FDA, and regulatory standards.
  • Strong attention to detail, documentation accuracy, and analytical skills.
  • Ability to work independently and communicate effectively across departments.
  • Flexibility to support other shifts or tasks as business needs arise.