ZipRecruiter

Log In

1

Quality Associate Jobs in Madison, WI (NOW HIRING)

United Alloy, Inc.

Quality Engineer

Janesville, WI · On-site

$64K - $82K/yr

Certified Quality Engineer (CQE), Certified Six Sigma Green Belt (CSSGB) or Certified Quality Improvement Associate (CQIA) • Solid understanding of quality systems, inspection and testing processes ...

Camaco

QUALITY SUPERVISOR

Portage, WI

Qualifications Required Education & Experience 1. Associates Degree in Engineering, a related ... quality assurance. 4. Experience in automotive seating. Competencies 1. Technical Capacity 2. ...

Adecco

Quality Inspector - Whitewater

Whitewater, WI · On-site

$22/hr

Quality Inspector - 3rd Shift Whitewater, WI | $ 22.00/hour Adecco is currently recruiting an ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

Quality Inspector - Whitewater

Whitewater, WI

$22/hr

Quality Inspector - 3rd Shift Whitewater, WI | $ 22.00/hour Adecco is currently recruiting an ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

Quality Inspector - Whitewater

Whitewater, WI

$22/hr

Quality Inspector - 3rd Shift Whitewater, WI | $ 22.00/hour Adecco is currently recruiting an ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

previous pagenext page

Showing results 21-40

All JobsQuality Associate JobsQuality Associate Jobs in Madison, WI

Quality Associate information

See Madison, WI salary details

$11

$27

$51

How much do quality associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for quality associate in Madison, WI is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $18.41 and $31.73 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 Madison, WI? The most popular types of Quality jobs in Madison, WI are:
What are popular job titles related to Quality Associate jobs in Madison, WI? For Quality Associate jobs in Madison, WI, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Madison, WI look for? The top searched job categories for Quality Associate jobs in Madison, WI are:
What cities near Madison, WI are hiring for Quality Associate jobs? Cities near Madison, WI with the most Quality Associate job openings:
Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Madison, WI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $56,446 per year, or $27.1 per hour.

Senior Associate I - Quality Assurance

Catalent, Inc.

Madison, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 hours ago

Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

59th of 86 rated pharmaceutical

Job description

Senior Associate I - Quality Assurance Operations, Data Review
Position Summary:
• Work Schedule: Monday - Friday 8am-5pm
• 100% on-site
Catalent Madison is a pharmaceutical manufacturing site specializing in the development and production of high-quality drug products, with a strong focus on biologics and sterile injectables. The site supports global clients by delivering compliant, reliable, and scalable manufacturing solutions.
The Senior Associate I- Quality Assurance Operation, Data Review at Catalent Madison supports Quality Assurance across a broad range of functions to ensure compliance with FDA regulations and internal quality systems, directly contributing to the production of safe, high-quality biologic drug products. This position spans equipment management, document control, materials quality, training, investigations/CAPA, audits, and on-the-floor manufacturing support. The Senior Associate I- Quality Assurance Operations, Data Review requires close cross-functional collaboration to maintain inspection readiness, drive continuous improvement, and support end-to-end quality oversight from raw materials through final product release.
The Role:
  • Responsible for maintaining and enhancing the effectiveness of the Quality System through ensuring compliant preparation and execution of quality control operations.
  • Review analytical and microbiology data and documentation including raw data, test methods, protocols, and reports for accuracy, completeness, and compliance in a timely manner.
  • Review and report unusual or out-of-specification testing results
  • Review supporting documentation including laboratory records and associated documents to ensure traceability to raw data and verify all reagents, standards and equipment used are within the acceptance range.
  • Ensure analysts follow all applicable SOPs and CGMP regulations and work with analysts for document corrections and provide guidance accordingly.
  • Notifies Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.
  • Other duties as assigned.

The Candidate:
  • Master's degree in STEM discipline with minimum of 0 years related experience.
  • OR
  • Bachelor's Degree in STEM discipline with minimum of 3 years related experience.
  • OR
  • Associates Degree in STEM discipline with minimum of 6 years related experience.
  • OR
  • High School Diploma with a minimum of 7 years related experience.

Why you should join Catalent:
  • Potential for career growth on an expanding team
  • Abundance of cross-functional exposure to other areas within the organization
  • Opportunity to work globally
  • 152 hours of paid time off annually + 8 paid holidays
  • Day one benefits! Medical, dental, vision and 401K benefits effective on your first day

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.

What Catalent employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Catalent logo

About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

Social media

FacebookTwitter

View All Catalent Jobs

Apply