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Quality Associate Jobs in Tooele, UT (NOW HIRING)

Hunter Douglas

Quality Engineer

Salt Lake City, UT · On-site

$78K - $106K/yr

Develop and maintain effective quality management systems, including policies, procedures, and quality standards to ensure compliance with customer requirements and applicable regulations.

Torus, Inc.

Quality Engineer

Salt Lake City, UT · On-site

$69K - $90K/yr

About the Role The Quality Engineer is responsible for ensuring that all products, components, and sub- assemblies meet quality standards and customer specifications before they are shipped or moved ...

Flex Ltd.

Quality Engineer

Salt Lake City, UT · On-site

$69K - $90K/yr

Holds up Product Engineers and Quality Program Managers with customer interfaces as necessary on quality related issues. * Assures data availability and integrity for all quality related data.

Torus Inc.

Quality Engineer

Salt Lake City, UT · On-site

$60 - $80/hr

About the Role The Quality Engineer is responsible for ensuring that all products, components, and sub- assemblies meet quality standards and customer specifications before they are shipped or moved ...

TekCommands Inc

Quality Engineer

Draper, UT · On-site

$67K - $86K/yr

Investigate moderately complex manufacturing product quality and compliance issues which may include: - Investigate PRAs and complaints for manufacturing related issues - Manage site NCRs, CAPAs ...

Northrop Grumman

Engineer Quality

Salt Lake City, UT · On-site

$72K - $108K/yr

Develops, modifies, applies and maintains quality evaluation and control systems and protocols for processing materials into partially finished or finished materials product. Collaborates with ...

Hexcel Corporation

Quality Engineer

West Valley City, UT

$69K - $89K/yr

Quality Engineers at Hexcel drive fundamental changes in the way we work. Our Quality Engineers are highly visible to all levels of the organization, leading cross functional teams to analyze risks ...

Hexcel Corporation

Quality Engineer

Salt Lake City, UT · On-site

$69K - $90K/yr

Quality Engineers at Hexcel drive fundamental changes in the way we work. Our Quality Engineers are highly visible to all levels of the organization, leading cross functional teams to analyze risks ...

Hexcel Corporation

Quality Engineer

Salt Lake City, UT · On-site

$69K - $90K/yr

Quality Engineers at Hexcel drive fundamental changes in the way we work. Our Quality Engineers are highly visible to all levels of the organization, leading cross functional teams to analyze risks ...

Mars, Incorporated

QA Technician

Salt Lake City, UT · On-site

Job Summary The Quality Assurance Technician ensures the safety, quality, and consistency of ... Associate degree (A.A.) or equivalent from a two-year college or technical school; or * Six months ...

Astrix Inc

QA Supervisor- Food

Salt Lake City, UT · On-site

$55K/yr

Associate or Bachelor's degree in Food Science, Microbiology, or a related field preferred * Bilingual preferred * 5+ years of experience in a QA or food safety role within a food manufacturing ...

L3HHCM20

Specialist, Quality Engineer

Salt Lake City, UT

$69K - $89K/yr

Specialist, Quality Engineer Job Code: 41397 Job Location: Salt Lake City: On-site Job Schedule: 9/80, Off Every other Friday, 1st Shift Job Decription: The Program Quality Engineer function is a ...

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All JobsQuality Associate JobsQuality Associate Jobs in Tooele, UT

Quality Associate information

See Tooele, UT salary details

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$47

How much do quality associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for quality associate in Tooele, UT is $25.29, according to ZipRecruiter salary data. Most workers in this role earn between $17.16 and $29.57 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.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Tooele, UT?

The most popular types of Quality jobs in Tooele, UT are:

What cities near Tooele, UT are hiring for Quality Associate jobs?

Cities near Tooele, UT with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Tooele, UT as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $52,593 per year, or $25.3 per hour.

Quality Engineer

Stark Pharma Solutions Inc

West Valley City, UT • On-site

$69K - $89K/yr

Contractor

Re-posted 11 days ago

Job description

Hi,

My name is Sravani Dasari, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Quality Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows.

Job Title: Quality Engineer
Location: West Valley City, UT
Duration: Long Term

Position Overview

We are seeking an experienced Quality Engineer to support new product development, design quality, and remediation initiatives within a medical device environment. The ideal candidate will possess strong technical expertise in traceability matrix verification (TMV), risk management, verification and validation (V&V), and design integration activities. This role requires hands-on experience developing and executing quality engineering activities while ensuring compliance with applicable regulatory requirements.

Key Responsibilities

• Support new product development and design quality activities throughout the product lifecycle.
• Develop and execute traceability matrix verification (TMV), risk management, and verification & validation (V&V) activities.
• Participate in design integration and design remediation initiatives to ensure product quality and regulatory compliance.
• Support Design History File (DHF) remediation and documentation updates.
• Implement Design for Manufacturing (DFM) principles and support risk management architecture.
• Collaborate with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, and Quality Assurance.
• Ensure compliance with FDA Quality System Regulations and internal quality procedures.
• Contribute to continuous improvement initiatives and quality system enhancements.

Required Qualifications

• Bachelor's Degree in Engineering or a related technical discipline.
• 4+ years of Quality Engineering experience within the medical device industry.
• Experience in New Product Development (NPD) and Design Quality activities.
• Strong knowledge of FDA 21 CFR Part 820 and medical device quality system requirements.
• Hands-on experience developing and executing TMV, Risk Management, and Verification & Validation (V&V) activities.
• Experience with Design Integration, Design Remediation, and Design History File (DHF) remediation.
• Knowledge of Design for Manufacturing (DFM) principles and risk management methodologies.
• Experience with vascular medical devices such as catheters, stents, guidewires, or related products is highly preferred.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/