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Quality Associate Jobs in Bloomington, IN (NOW HIRING)

PMG Indiana

Quality Engineer

Columbus, IN · On-site

$67K - $86K/yr

Reports quality system performance to management for review as a basis for improvement of internal systems.Visits customers, vendors or job shop sites for quality issues, performance analysis, and/or ...

PMG Indiana Corporation

Quality Engineer

Columbus, IN · On-site

$67K - $86K/yr

Reports quality system performance to management for review as a basis for improvement of internal systems. Visits customers, vendors or job shop sites for quality issues, performance analysis, and ...

SAIC

Quality Assurance Technician III

Bedford, IN

Quality Assurance Subcategory: Qual Assurance Technician Schedule: Full-Time Shift: Day Job Travel ... Associate's degree in related discipline and 3 years or more of related experience; or high school ...

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Quality Associate information

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How much do quality associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for quality associate in Bloomington, IN is $23.61, according to ZipRecruiter salary data. Most workers in this role earn between $16.01 and $27.60 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.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Bloomington, IN?

The most popular types of Quality jobs in Bloomington, IN are:

What job categories do people searching Quality Associate jobs in Bloomington, IN look for?

The top searched job categories for Quality Associate jobs in Bloomington, IN are:

What cities near Bloomington, IN are hiring for Quality Associate jobs?

Cities near Bloomington, IN with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Bloomington, IN as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $49,101 per year, or $23.6 per hour.

Quality Associate 2 - Batch Release

Singota Solutions

Bloomington, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description


Why join Team Singota?
We pride ourselves on a high-trust, high-accountability environment where we lift each other up. When you join Singota, you are a part of a team that respects, supports, and values its people. We celebrate wins together, brainstorm solutions together, and genuinely enjoy the work we do. The result? A team that's not just efficient, but also passionate, dedicated, and fun to work with.
Job Title: Quality Associate 2 - Batch Release
Department: QA
Reports to: Quality Assurance Supervisor
Location: Bloomington, IN (Onsite)
Position Type: Full-time, Exempt, 40 hr/wk
General Description:
The Quality Associate 2 - Batch Release is responsible for managing the workflow of records for Manufacturing and
QC/Development activities in accordance with company, client and regulatory quality standards, including the
appropriate disposition of materials or manufactured product. This position is responsible for reviewing records for
accuracy and completeness and for identifying discrepancies or issues that could result in product impact.
1. Responsible for the issuance, review, and release of batch records and protocols. Ensure records are executed in accordance with procedures and regulatory requirements.
2. Perform disposition of materials within the electronic inventory management system, issue appropriate release documentation.
3. Collaborate with various departments to ensure record specifications are accurate and related deviations are thoroughly investigated.
4. Interface with clients to provide support for review and release of records related to client material or product.
5. Author complex deviations, CAPAs, and change controls as needed.
6. Participate in the training of new Quality Assurance staff.
7. Support continuous improvement of the site's Quality Systems.
8. Generate and issue controlled labeling material for manufacturing operations. Review for legibility, accuracy, and compliance to company, client, and regulatory standards.
9. Review and disposition Quality Control/Development Laboratory records.
10. Write and review Standard Operating Procedures related to Quality Systems within Manufacturing and QC/Development.
11. Responsible for the development and issuance of Quality operational metrics.
12. Represent Quality Assurance at various project and technical meetings.
13. Must perform other duties as assigned by supervision. Responsible for notifying supervision when issues arise.
14. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures
Requirements
Skills and Physical Activity Requirements:
1. Excellent internal and external communication.
2. Demonstration of positive attitude and professional presence.
3. Good time management and organizational skills.
4. Detail orientated, must be able to perform thorough reviews of documentation.
Education and Work Experience Requirements:
1. Bachelor's degree or equivalent work experience - science related field preferred.
2. Minimum 3-5 years pharmaceutical experience, preferably in a Quality role.
3. Must possess knowledge of Good Documentation Practices (GDP).
4. Experience in an aseptic manufacturing and laboratory operations is desirable.
Benefits
  • Dental insurance - effective day one of employment
  • Health insurance - effective day one of employment
  • Vision insurance - effective day one of employment
  • Health savings account
  • Life & AD&D insurance
  • Short & long term disability
  • Paid time off & holidays
  • Employee Assistance Program
  • Tuition assistance
  • Sam's Club Basic membership reimbursement
  • 401(k) with company match

Singota Solutions is an Equal Opportunity Employer

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