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Quality Control Associate Jobs in Utah (NOW HIRING)

... quality control programs to specifications. Interprets manufacturing drawings, diagrams ... Associates Degree with a minimum of 2 years of prior related experience. Preferred Additional ...

A dedicated and motivated individual to join our production team as a Production Associate. In this ... quality control. * Follow standard operating procedures (SOPs) and safety guidelines to ensure a ...

A dedicated and motivated individual to join our production team as a Production Associate. In this ... quality control. * Follow standard operating procedures (SOPs) and safety guidelines to ensure a ...

A dedicated and motivated individual to join our production team as a Production Associate. In this ... quality control. * Follow standard operating procedures (SOPs) and safety guidelines to ensure a ...

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Quality Control Associate information

See Utah salary details

$10

$23

$34

How much do quality control associate jobs pay per hour?

As of May 29, 2026, the average hourly pay for quality control associate in Utah is $23.18, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $28.22 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Quality Control Associate, and why are they important?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges Quality Control Associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What does a Quality Control Associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

Which is higher position, QA or QC?

In the context of a Quality Control Associate role, Quality Assurance (QA) is generally considered a higher-level function that focuses on preventing defects through process improvements, while Quality Control (QC) involves inspecting products to identify defects. QA roles often involve more strategic responsibilities and may require broader skills or certifications, whereas QC is more about testing and inspection tasks. The hierarchy can vary by organization, but QA typically holds a higher or more senior position than QC.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Utah? The most popular types of Quality Control jobs in Utah are:
What are popular job titles related to Quality Control Associate jobs in Utah? For Quality Control Associate jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Quality Control Associate jobs in Utah look for? The top searched job categories for Quality Control Associate jobs in Utah are:
What cities in Utah are hiring for Quality Control Associate jobs? Cities in Utah with the most Quality Control Associate job openings:
What are popular job titles related to Quality Control Associate jobs in UT? For Quality Control Associate jobs in UT, the most frequently searched job titles are:

Quality Assurance Specialist

Aspen Co-Pak LLC

Spanish Fork, UT

Full-time

Posted 22 days ago


Job description

The Quality Assurance Specialist supports the Quality Managerin maintaining Aspen Co-Pak’s compliance with cGMP, FDA (21 CFR 111/117),NSF/455-2, Organic, Kosher, and customer quality requirements. This position isresponsible for documentation control, MMR creation and review, specificationsmanagement, COA verification, environmental monitoring, internal auditing, andsupporting quality programs such as CAPA, complaints, and supplier approval.The QA Specialist ensures accurate records, strong GMP compliance, andeffective execution of key quality system processes.


Job Duties

  • Create, review, revise, and maintain:
    • Master Manufacturing Records (MMRs)
    • Product Specifications (raw material, bulk, finished product)
    • SOPs, logs, forms, and controlled documents
  • Maintain document control system, ensuring proper version control and distribution.
  • Support the development and improvement of quality system procedures.
  • Receive, review, and verify Certificates of Analysis (COAs) for raw materials, premixes, bulk products, and finished goods.
  • Ensure COA compliance with internal specifications and customer requirements.
  • Submit samples to third-party laboratories, track testing results, and maintain testing logs.
  • Maintain retain samples as required by procedure.
  • Execute the Environmental Monitoring Program (swabs, ATP, air/water sampling).
  • Document and trend EMP results; report any deviations.
  • Conduct internal audits per schedule; document findings and follow up on corrective actions.
  • Assist in external audits (customer, regulatory, certifying bodies).
  • Assist with CAPA investigations, root cause analysis, corrective/preventive action implementation, and verification.
  • Support customer complaint investigations, documentation, and corrective action follow-up.
  • Maintain the Supplier Approval Program by collecting documents, verifying certifications, and updating files.
  • Participate in traceability exercises, mock recalls, and emergency management drills.
  • Support hazard analysis and risk assessments for processes and materials.
  • Support GMP compliance through floor checks, gowning verification, documentation reviews, and hygiene monitoring.
  • Work with warehouse software such as Data Ninja to verify inventory, lot tracking, and FIFO compliance.
  • Collaborate with production and warehouse teams to ensure adherence to SOPs and quality standards.
  • Perform other duties as assigned by the Quality Manager.

Required Skills

  • Has strong knowledge and skills associated with Quality Assurance systems and procedures in food and dietary supplement manufacturing
  • Strong understanding of cGMP and FDA regulations (21 CFR 111/117).
  • Ability to read, interpret, and create technical documents (MMRs, specs, COAs, SOPs).
  • Excellent documentation, organization, and recordkeeping skills.
  • Proficiency in Microsoft Excel, Word, and PDF editing tools.
  • Ability to use or learn warehouse/data systems such as Data Ninja.
  • Strong attention to detail, accuracy, and problem-solving skills.
  • Effective communication skills (written and verbal).
  • Ability to work independently and in a team environment.
  • Strong time-management and multitasking abilities.
  • Communicates effectively and professionally. Ability to speak and write English with good writing skills, Spanish speaking/writing is a plus

Experience and Education

  • Experience as a Quality assurance
  • High school diploma or GED.
  • 2-5 years of experience in Quality Assurance or Quality Control in food, dietary supplements, or cosmetic manufacturing.
  • Experience with documentation review, COA verification, and GMP compliance.
  • Experience working with NSF, SQF, Organic, Kosher, Halal certification requirements

Preferred

  • Experience with Organic, Kosher, and/or NSF/455-2 certification programs.
  • Experience with Environmental Monitoring Programs and internal audits.
  • Knowledge of hazard analysis and risk assessment.
  • Experience with CAPA, supplier approval, and customer complaint investigations.
  • Bilingual English/Spanish is strongly preferred at Aspen Co-Pak.
  • Associate’s or Bachelor’s degree in a science-related field (Food Science, Biology, Chemistry, etc.) a plus

Physical Requirements

  • Ability to lift up to 30 lbs.
  • Ability to stand, walk, and move between production, warehouse, and office areas.
  • Ability to work in a manufacturing environment requiring PPE.