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Quality Associate Jobs in Frisco, TX (NOW HIRING)

Quality Assurance is responsible for keeping the press supplied with raw materials, tools, and inks to print the jobs. They are also responsible for quality control and keeping the production floor ...

Quality Assurance Associate

Fort Worth, TX · On-site

$21.60 - $25.10/hr

As a Quality Assurance Associate at Sam's Club Supply Chain, you will play a vital role in ensuring the quality and accuracy of our warehouse inventory. You must be comfortable working in extreme ...

Quality Assurance Associate

Fort Worth, TX · On-site

$21.60 - $25.10/hr

As a Quality Assurance Associate at Sam's Club Supply Chain, you will play a vital role in ensuring the quality and accuracy of our warehouse inventory. You must be comfortable working in extreme ...

Quality Engineer

Allen, TX · On-site

$67K - $86K/yr

Work independently without supervision and have the ability to mentor junior quality associates. Qualifications : * Bachelor of Science degree in a technical area such as science, engineering, math ...

As a Quality Control Associate, you'll be responsible for maximizing productivity, quality, and inventory accuracy while performing material movement functions throughout the Arteriors. To land this ...

As a Quality Control Associate, you'll be responsible for maximizing productivity, quality, and inventory accuracy while performing material movement functions throughout the Arteriors. To land this ...

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Quality Associate information

See Frisco, TX salary details

$10

$25

$47

How much do quality associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality associate in Frisco, TX is $25.21, according to ZipRecruiter salary data. Most workers in this role earn between $17.12 and $29.47 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 Frisco, TX?

The most popular types of Quality jobs in Frisco, TX are:

What are popular job titles related to Quality Associate jobs in Frisco, TX?

For Quality Associate jobs in Frisco, TX, the most frequently searched job titles are:

What cities near Frisco, TX are hiring for Quality Associate jobs?

Cities near Frisco, TX with the most Quality Associate job openings:

Infographic showing various Quality Associate job openings in Frisco, TX as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 21% Part Time, 13% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $52,430 per year, or $25.2 per hour.

Sr Clinical Quality Associate

Arnex Solutions LLC

Plano, TX • On-site

Other

Posted 2 days ago

New


Job description

Associate, Maple grove, MN, Sylmar, CA, Santa Clara, CA, Plano, TX Role Summary    

The Senior Clinical Quality Associate supports clinical affairs personnel globally in ensuring compliance with medical device and Google Cloud Platform regulations and standards, as well as applicable company policies and procedures. This role spans study support, CAPA management, and internal/external audit preparation and execution.

Key Responsibilities    

•       Reviews study documents for compliance with applicable regulations, standards, and internal procedures.

•       Acts as a compliance resource to clinical study teams regarding applicable regulations, standards, and procedures.

•       Supports compliant execution of clinical research projects.

•       Generates CAPA documentation including investigations, resolution plans, and implementation reports; drives resolution cross-functionally.

•       Drives continuous process improvement and ensures work complies with regulatory and compliance standards.

•       Serves as a key player in preparation and overall support for internal and external audits, including responding to audit findings through the CAPA process.

•       May perform internal compliance assessments and/or audits.

•       Supports project teams in preparation for regulatory authority inspections or audits.

•       May support additional clinical quality tasks as needed.

Required Qualifications    

•       Bachelor’s degree in a related field, or an equivalent combination of education and work experience.

•       Minimum 4 years of related work experience with a solid understanding of clinical quality or Google Cloud Platform compliance functions.

•       Strong understanding of Good Clinical Practice (Google Cloud Platform) including U.S. regulations (21 CFR Parts 50, 54, 56, 812) and international standards (ISO 14155).

•       Strong written communication skills and independent decision-making ability.

•       Effective problem-solving and planning skills; able to work independently under minimal supervision.

Preferred Qualifications    

•       Minimum 5 years of experience in medical devices, clinical research, or a related industry.

•       Minimum 3 years in a quality role within a medical device or clinical trial environment.

•       Google Cloud Platform audit experience strongly preferred.