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Quality Associate Jobs in Indiana (NOW HIRING)

Langham Logistics

Quality Supervisor

Whitestown, IN · On-site

The Associate Manager ensures that cleanroom and sampling activities are performed under controlled conditions, safeguarding product integrity and preventing cross-contamination. In addition to ...

Langham Logistics

Quality Supervisor

Plainfield, IN

The Associate Manager ensures that cleanroom and sampling activities are performed under controlled conditions, safeguarding product integrity and preventing cross-contamination. In addition to ...

Langham Logistics

Quality Supervisor

Whitestown, IN · On-site

The Associate Manager ensures that cleanroom and sampling activities are performed under controlled conditions, safeguarding product integrity and preventing cross-contamination. In addition to ...

Langham Logistics

Quality Supervisor

Plainfield, IN · On-site

The Associate Manager ensures that cleanroom and sampling activities are performed under controlled conditions, safeguarding product integrity and preventing cross-contamination. In addition to ...

INCOG

QA Associate

Fishers, IN · On-site

The QA Associate will need to provide support with identifying operational and quality gaps. The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing ...

fng

Manufacturing Quality Coordinator

Veedersburg, IN · On-site

Support manufacturing in the development of job instructions and maintain and train quality associates on quality related job instructions and procedures. * Lead auditor for quality systems. * May be ...

fng

Manufacturing Quality Coordinator

Veedersburg, IN · On-site

Support manufacturing in the development of job instructions and maintain and train quality associates on quality related job instructions and procedures. * Lead auditor for quality systems. * May be ...

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All JobsQuality Associate JobsQuality Associate Jobs in Indiana

Quality Associate information

See Indiana salary details

$10

$25

$48

How much do quality associate jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for quality associate in Indiana is $25.63, according to ZipRecruiter salary data. Most workers in this role earn between $17.40 and $29.95 per hour, depending on experience, location, and employer.

Is QA a difficult job?

Quality Associate roles can be challenging as they require attention to detail, understanding of quality standards, and often involve repetitive tasks and strict compliance requirements. Success in the role depends on strong analytical skills, knowledge of testing procedures, and sometimes certifications like Six Sigma or ISO standards.

Is QC a high paying job?

Quality Associate positions typically offer average salaries that are competitive within manufacturing and production industries, but they are generally not considered high-paying roles. Salary levels depend on factors such as experience, location, and industry, with some roles offering opportunities for advancement and certification that can increase earning potential.

What are Quality Associates?

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 jobs pay 10,000 a month without a degree?

A Quality Associate typically earns less than $10,000 a month, but high-paying roles in sales, real estate, or skilled trades can reach or exceed that level without a degree. These jobs often require experience, certifications, or specialized skills and may involve variable income or commission-based pay structures.

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 is the job of a quality associate?

A quality associate is responsible for inspecting products, monitoring manufacturing processes, and ensuring compliance with quality standards. They often use testing tools and follow procedures to identify defects and improve product quality. Strong attention to detail and knowledge of quality management systems are essential for this role.

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 Indiana? The most popular types of Quality jobs in Indiana are:
What are popular job titles related to Quality Associate jobs in Indiana? For Quality Associate jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Indiana look for? The top searched job categories for Quality Associate jobs in Indiana are:
What cities in Indiana are hiring for Quality Associate jobs? Cities in Indiana with the most Quality Associate job openings:
Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Indiana as of June 2026, with employment types broken down into 2% As Needed, 56% Full Time, 32% Part Time, 1% Temporary, and 9% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $53,305 per year, or $25.6 per hour.
MQA Associate (2nd or 3rd Shift Available)

MQA Associate (2nd or 3rd Shift Available)

Aquestive Therapeutics

Portage, IN • On-site

Full-time

Posted 19 days ago

Job description

Job Summary:
The Manufacturing Quality Associate is responsible for ensuring quality and compliance during the day-to-day operations in the manufacturing environment by partnering with operations, supply chain, engineering, quality control, or other functions to support product quality. This role provides GMP oversight through guidance against internal SOPs, WI, Protocols and Records as it pertains to manufacturing activities for development and commercial manufacturing.
Responsibilities:
  • Monitors all operations pertaining to manufacturing to ensure adherence to AQST policies and procedures and provides guidance and clarity to colleagues to ensure consistent approaches to product quality are applied.
  • Conducts routine internal audits and facility walkthroughs to ensure compliance with internal quality system requirements and to maintain a state of audit readiness.
  • Initiates and investigates nonconformances, project managing to resolve quality issues by partnering with other functions.
  • Author and review Forms, Batch Records, WI, SOPs, Protocols in electronic document management system.
  • Investigates assigned product quality complaints utilizing knowledge of the manufacturing and quality processes at Aquestive.
  • Owns CAPA records and action item implementation, partnering with operations, supply chain, engineering, and QC staff to ensure corrective actions are implemented according to approved timelines and ensuring their effectiveness post-implementation.
  • Coordinates the Environmental Monitoring program including scheduling of third-party water testing, sampling, and report generation
  • Short to medium term (3-12 months) project owner for quality projects to improve efficiency or compliance profile
  • Understands the manufacturing schedule and provides quality support to ensure business continuity and seamless transitions between manufacturing stages.
  • Operates with a sense of urgency in a fast-paced environment.
  • Performs real time review of operational records, including Batch Records, and assists in obtaining any required corrections.
  • Performs AQL Testing on finished product by verifying various attributes such as product appearance, product and packaging dimensions, presence and accuracy of printing on strip and pouch, and seal integrity.
  • Performs line clearances for all steps of the manufacturing process.
  • Reviews, assesses, and archives pest control documents.
  • Maintains QA Retain Program, including sampling, inventory management and inspections required per internal SOPs.
  • Leads process for ensuring manufacturing environment is in a state of control through the evaluation of the building automated system software, in partnership with Maintenance.
  • Determines, documents and communicates when facility may be released back to cGMP operations after a shutdown, environmental excursion, etc.
  • Performs other duties as instructed by quality management.
  • Acknowledges that this position requires off-hours and weekend work from time to time to assure adequate QA floor support.

Qualifications:
  • BS degree required preferably in chemistry, biochemistry, or related science field.
  • 5+ years of related experience in the pharmaceutical, biotechnology, or medical device industry responsibility preferred.
  • Demonstrated knowledge of quality systems, GMPs, industry standards, and regulatory requirements for the manufacture, testing, and release of pharmaceutical products.
  • Formal training in Quality disciplines (auditing, engineering, process improvement) as demonstrated through certification (ASQ, Lean Six Sigma, etc) highly preferred
  • Technical proficiency at reviewing/auditing production records, reports and/or GMP related documentation.
  • Ability to work within a team environment and willingness to contribute to the overall goals of the company.
  • Ability to lead project teams
  • Ability to handle multiple assignments and projects with competing priorities while independently managing time is critical.
  • Good organizational skills, high level of attention to detail, excellent oral and written communication skills with the ability to interact at all levels.
  • Ability to lift up to 35lbs.
  • Must be willing to work off hour shifts and weekends as necessary.

The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position. This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary.
As part of Aquestive's employment process, final candidate will be required to complete a drug test and background check prior to employment commencing. Please Note: Aquestive is a drug-free workplace and has a drug free workplace policy in place.
Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate's relevant skills, experience, and education.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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