ZipRecruiter

Log In

1

Quality Associate Jobs in Clearfield, UT (NOW HIRING)

Spirax-Sarco Engineering

Quality, Supervisor

Ogden, UT · On-site

Associate or Bachelor's degree in Quality, Engineering, Manufacturing, Business, or a related field preferred; equivalent relevant experience will be considered. * 3+ years of quality experience in a ...

Chromalox

Quality, Supervisor

Ogden, UT · On-site

Associate or Bachelor's degree in Quality, Engineering, Manufacturing, Business, or a related field preferred; equivalent relevant experience will be considered. * 3+ years of quality experience in a ...

Chromalox, Inc.

Quality, Supervisor

Ogden, UT · On-site

Associate or Bachelor's degree in Quality, Engineering, Manufacturing, Business, or a related field preferred; equivalent relevant experience will be considered. * 3+ years of quality experience in a ...

Chromalox, Inc.

Quality, Supervisor

Ogden, UT · On-site

Associate or Bachelor's degree in Quality, Engineering, Manufacturing, Business, or a related field preferred; equivalent relevant experience will be considered. * 3+ years of quality experience in a ...

Spirax-Sarco Engineering

Quality, Supervisor

Ogden, UT · On-site

Associate or Bachelor's degree in Quality, Engineering, Manufacturing, Business, or a related field preferred; equivalent relevant experience will be considered. * 3+ years of quality experience in a ...

Unicon Pharma Inc.

Quality Analyst I

Salt Lake City, UT · On-site

Quality Auditor Associate 1st shift early (6 a.m. - 2:30 p.m. M-F) 5 Months (possible extension) Salt Lake City, UT Screenings: The QA roles WILL require the physical please, as a lot of their work ...

Unicon Pharma Inc.

Quality Analyst I

Salt Lake City, UT · On-site

$33 - $35/hr

Job Title: Quality Auditor Associate Location: Salt Lake City, UT Duration: 6 Months Contract Shift: 3rd shift (10 p.m. - 6:30 a.m. M-F, Onsite) Description: The job requirements include the ...

Hunter Douglas

Quality Engineer

Salt Lake City, UT · On-site

$78K - $106K/yr

Implement quality tools, such as Statistical Process Control (SPC) and Failure Mode and Effects Analysis (FMEA), to identify and prevent defects in production. * Oversee all quality control ...

OmniForce

Quality Engineer

Salt Lake City, UT · On-site

$69K - $90K/yr

They're seeking a Quality Engineer to join their team in St. George, UT. Eligible candidates will need to be local to the St. George, UT area or open to relocating. Benefits: Competitive compensation ...

Autoliv United States

Quality Engineer

Ogden, UT · On-site

$70 - $110/hr

This is why we can never compromise on quality. We are working to increase vehicle safety by developing seatbelts, airbags and steering wheels and you can be part of our team as ROLE . In this role ...

Autoliv United States

Quality Engineer

Ogden, UT · On-site

$70K - $91K/yr

This is why we can never compromise on quality. We are working to increase vehicle safety by developing seatbelts, airbags and steering wheels and you can be part of our team as ROLE . In this role ...

next page

Showing results 1-20

All JobsQuality Associate JobsQuality Associate Jobs in Clearfield, UT

Quality Associate information

See Clearfield, UT salary details

$10

$25

$47

How much do quality associate jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for quality associate in Clearfield, UT is $25.10, according to ZipRecruiter salary data. Most workers in this role earn between $17.02 and $29.38 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 Clearfield, UT?

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

What job categories do people searching Quality Associate jobs in Clearfield, UT look for?

The top searched job categories for Quality Associate jobs in Clearfield, UT are:

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

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

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Clearfield, UT as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $52,217 per year, or $25.1 per hour.

Senior Staff Clinical Quality Associate (Onsite)

Salt Lake City, UT

Stryker
Medical Equipment and Supplies Manufacturing • 10K+ employees

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

130th of 495 rated machine equipment manufacturers

Great coworkers

People enjoy working here

Good employer

Learn more about Strykerexternal

$143K - $238K/yr

Full-time

Posted 29 days ago

Job description

Work Flexibility: Hybrid or Onsite

Stryker is hiring a Senior Staff Clinical Quality Associate for our Neurovascular division. This is an onsite role based in Fremont, CA or Salt Lake City, UT.

As the Senior Staff Clinical Quality Associate, you will focus on clinical quality, compliance governance, and regulatory readiness across global clinical research activities. You will provide oversight of quality systems, compliance programs, audits, inspections, and clinical processes to ensure clinical services, documentation, and operations align with applicable regulations and quality standards. You will work across functions to identify risks, strengthen controls, and support the continuous improvement of clinical quality programs.

This role provides quality and compliance oversight for clinical research activities, ensuring processes, documentation, systems, and vendor operations remain compliant, inspection-ready, and aligned with global regulatory and quality requirements.

What you will do

  • Manage clinical quality and compliance programs, establishing milestones, resource plans, and delivery timelines to support on-time execution

  • Identify, assess, and communicate compliance risks and control strategies to stakeholders across clinical, quality, and business functions

  • Lead internal and external audit and inspection activities, including preparation, execution, follow-up actions, and documentation management

  • Participate in regulatory inspections, including inspections of clinical studies conducted by regulatory authorities

  • Conduct vendor audits and inspections, maintain audit schedules, and monitor supplier compliance with quality requirements

  • Analyze process deviations, determine corrective actions, and update procedures to maintain compliance with applicable regulations and standards

  • Develop, maintain, and revise standard operating procedures, work instructions, and quality documentation

  • Deliver compliance training, provide guidance on clinical quality requirements, and support continuous improvement initiatives across the clinical organization

What you need

Required

  • Bachelor's degree

  • Minimum 7 years of experience in clinical quality, clinical research, quality assurance, compliance, or a related regulated healthcare or life sciences field

  • Minimum 5 years of experience supporting quality systems, regulatory compliance programs, audits, or inspections

  • Experience supporting clinical studies conducted within a regulated environment

Preferred

  • Experience in medical device, pharmaceutical, biotechnology, or clinical research industries

  • Experience participating in regulatory inspections and audit readiness activities

  • Experience developing and maintaining standard operating procedures and quality system documentation

  • Certified Quality Auditor (CQA), Regulatory Affairs Certification (RAC), or comparable quality or compliance certification

  • US5: $115,600 - $192,600 USD Annual
  • US30: $143,100 - $238,400 USD Annual
Travel Percentage: 30%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

What Stryker employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply