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Quality Associate Jobs in Utah (NOW HIRING)

New Balance

Quality Inspector

Salt Lake City, UT · On-site

$18.70 - $23.35/hr

We foster a culture in which every associate feels welcomed and respected, where leaders and ... You will be part of a team of quality inspectors focused on reducing the amount of defective ...

Route 92 Medical Inc

Quality Manager

West Jordan, UT · On-site

$130K - $150K/yr

Oversee development and execution of quality assurance test protocols. * Identify and plan ... Associate's degree + 8 yrs of medical device experience * Bachelor's degree + 7 yrs of medical ...

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 ...

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Quality Associate information

See Utah salary details

$10

$24

$46

How much do quality associate jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for quality associate in Utah is $24.52, according to ZipRecruiter salary data. Most workers in this role earn between $16.63 and $28.65 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 Utah? The most popular types of Quality jobs in Utah are:
What are popular job titles related to Quality Associate jobs in Utah? For Quality Associate jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Utah look for? The top searched job categories for Quality Associate jobs in Utah are:
What cities in Utah are hiring for Quality Associate jobs? Cities in Utah with the most Quality Associate job openings:
Quality Associate jobs near you
Associate Director, Quality Assurance (QA)

Associate Director, Quality Assurance (QA)

Denali Therapeutics

Salt Lake City, UT • On-site

Full-time

Medical, Retirement

Posted 3 days ago

Job description

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.

Based in Salt Lake City (SLC), the Associate Director, Quality Assurance (QA) will drive quality assurance defined strategies and objectives for a new large molecule drug substance clinical and commercial manufacturing facility. This includes manufacturing and analytical testing operations, ensuring compliance with FDA, EMA, and global regulatory requirements. This role manages a team responsible for key quality systems including batch disposition, deviations, CAPA, change control, and investigations. The position also partners with Manufacturing, QC, and CMC teams to maintain product quality, data integrity, and inspection readiness. The Associate Director, Quality also drives continuous improvement and fosters a strong culture of GMP compliance and operational excellence.

Key Accountabilities/Core Job Responsibilities:

  • Lead, mentor, and develop a team of quality professionals, fostering a strong culture of GMP compliance, accountability, and continuous improvement. Includes leading direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.

  • Provide strategic leadership to strengthen site quality systems and elevate overall regulatory compliance across manufacturing and testing operations.

  • Provide quality oversight for GMP manufacturing and QC laboratory operations to ensure adherence to FDA, EMA, and global regulatory standards.

  • Review and approve batch records and supporting documentation to support timely and compliant batch disposition and product release.

  • Lead and oversee the management of quality events, including deviations, investigations, CAPA, and change controls to ensure effective root cause analysis and corrective actions.

  • Maintain hands-on leadership and subject matter expertise in GMP quality operations, ensuring effective implementation and continuous improvement of the QMS.

  • Provide on-the-floor quality support to manufacturing operations to ensure real-time compliance and rapid resolution of quality issues.

  • Provide quality oversight for qualification and validation activities, including process validation, equipment qualification, and validation lifecycle management.

  • Partner cross-functionally with Manufacturing, Quality Control, Validation, and Regulatory teams to drive quality operations, inspection readiness, and continuous process improvement.

Qualifications/Skills:

  • Bachelor's degree in a core scientific discipline

  • Typically 9+ years of overall work experience, to include 5+ years in Biotech Manufacturing / Quality as well as 5+ years of people management experience

  • Familiarity with large molecule drug substance GMP manufacturing and testing

  • Knowledge of current USP/Ph. Eur./FDA/ISO/GMP standards and guidance

  • Ability to work independently or in team environments under deadlines

  • Excellent verbal and written communication skills

  • Ability to closely follow quality standards and company quality expectations

  • Strong collaboration and influencing skills

  • Strategic thinking combined with excellence in execution

  • Ability to learn quickly, driven by high curiosity

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more athttps://www.denalitherapeutics.com/careers

Thiscompensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.

Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

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