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Quality Associate Jobs in Geneva, IL (NOW HIRING)

The Quality Technician will ensure that LifeSpice proprietary blends meet all quality and ... Associate or bachelor's degree in a science-related field preferred Ability to participate in daily ...

The associate in this job has the responsibility to report, in a timely manner, Food Safety and Quality problems to personnel with authority to initiate action on those problems. * Follow all company ...

Quality Manager

West Chicago, IL · On-site

$100K - $130K/yr

Will ensure that the quality of all products produced within the production facility will be done ... Create a positive working environment for all associates; one that supports continuous improvement ...

Quality Manager

West Chicago, IL · On-site

$100K - $130K/yr

Will ensure that the quality of all products produced within the production facility will be done ... Create a positive working environment for all associates; one that supports continuous improvement ...

Quality Technician

Wheeling, IL · On-site

$22 - $24/hr

High school diploma or equivalent required; technical certificate, associate degree, or quality certification (ASQ CQT, ISO internal auditor) preferred. Working Conditions Production floor ...

QUALITY COORDINATOR

Woodridge, IL · On-site

$60K - $65K/yr

Associate degree preferred; with three or more years of quality systems experience. * Must have working knowledge of ISO 9001:2015 and ISO 14001:2015. * Experience with creating, updating, and ...

Retail Warehouse Associate

Elgin, IL · On-site

$14.75 - $16.25/hr

Retail Warehouse Associate Overview Since 1945, our client has built a strong foundation through ... This role plays a key part in maintaining efficiency, safety, and quality standards. Benefits

Retail Warehouse Associate

Chicago, IL · On-site

$15.50 - $17/hr

Retail Warehouse Associate Overview Since 1945, our client has built a strong foundation through ... This role plays a key part in maintaining efficiency, safety, and quality standards. Benefits

Retail Warehouse Associate

Chicago, IL · On-site

$15.50 - $17/hr

Retail Warehouse Associate Overview Since 1945, our client has built a strong foundation through ... This role plays a key part in maintaining efficiency, safety, and quality standards. Benefits

Showing results 21-40

Quality Associate information

See Geneva, IL salary details

$10

$26

$49

How much do quality associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for quality associate in Geneva, IL is $26.28, according to ZipRecruiter salary data. Most workers in this role earn between $17.84 and $30.72 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.

What are the most commonly searched types of Quality jobs in Geneva, IL? The most popular types of Quality jobs in Geneva, IL are:
What job categories do people searching Quality Associate jobs in Geneva, IL look for? The top searched job categories for Quality Associate jobs in Geneva, IL are:
What cities near Geneva, IL are hiring for Quality Associate jobs? Cities near Geneva, IL with the most Quality Associate job openings:
Infographic showing various Quality Associate job openings in Geneva, IL as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $54,672 per year, or $26.3 per hour.

Quality Assurance - Quality Engineer III

Viant

Wheeling, IL • On-site

$95K - $115K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Job description

Quality Assurance - Sr. Quality Engineer - Manufacturing
About the Site:
Our Wheeling facility combines precision machining and assembly capabilities to deliver high-quality medical device components and finished products.
We offer market competitive compensation. Potential salary range for this role is $95k-$115k. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. Onsite daily.
Benefits:
  • Medical, Dental, and Vision benefits, effective date of hire
  • 136 Hours PTO (prorated based on hire date) & 10 paid Holidays
  • Company-paid life insurance
  • 401k plan
  • Pet Insurance
  • Home Ownership
  • Tuition Reimbursement

About the Role
We are seeking a highly experienced and motivated Senior Quality Engineer to join our team. This role is critical in ensuring product quality and regulatory compliance throughout the design and manufacturing process. The ideal candidate will bring deep expertise in quality systems, process improvement, and cross-functional collaboration within a regulated industry, preferably medical devices.
What you'll do: Key Responsibilities
  • Adhere to company Core Beliefs and all safety and quality requirements, including, but not limited to company Quality Management System (QMS); Environmental, Health & Safety; company policies, procedures, and work instructions; and other relevant regulatory requirements.
  • Support regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
  • Monitor manufacturing of assigned products, ensuring compliance with DMR and quality system requirements, and ensure complete and correct Device History Records are maintained.
  • Identify, prioritize, and implement product and process improvement initiatives.
  • Review the adequacy and correctness of changes to Bills of Material (BOM's), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc.
  • Generate and lead the completion of protocols and reports for product, process, and test method validations.
  • Partner with Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommend process monitoring devices where required and/or appropriate.
  • Develop various inspection techniques and procedures to ensure product integrity to design specifications. Write and implement Incoming, In-Process, and Final Inspection procedures.
  • Ensure that the disposition of non-conforming materials comply with all relevant requirements and ensure that appropriate corrective actions are implemented to prevent recurrence.
  • Lead complaint investigations and manage appropriate remediation activities.
  • Review quality data for potential CAPA's, including analyses of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root cause analyses.
  • Assist with product transfers.
  • Work with suppliers, management, engineers, and manufacturing associates in the resolution of quality problems. Also, assist each of these groups with capability studies and the application of statistical quality control, including Cpk, DOE, Hypothesis Testing, etc.
  • Provide technical support and direct the work of Quality Inspectors, Quality Technicians, Training Specialists, and/or other Quality Engineers as needed.

Qualifications
Education:
  • Bachelor's degree in Engineering (Mechanical Engineering preferred) or a related discipline.

Experience:
  • Minimum 7+ years of Quality Assurance experience in a regulated manufacturing environment, preferably medical devices or other regulated industry.

Certifications (Preferred):
  • CQE, CRE, CQA, Six Sigma Green or Black Belt

Skills & Competencies
  • Strong knowledge of root cause analysis, DOE, statistics, lean manufacturing, risk management, and Six Sigma methodologies.
  • Proficient in Microsoft Office and Minitab.
  • Familiarity with metals processing and Toyota Production System is a plus.
  • Excellent interpersonal, written, and verbal communication skills.
  • Proven ability to work independently and manage multiple priorities.
  • Demonstrated success in driving continuous improvement and leading cross-functional teams.

Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life-enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn.
Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.