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Quality Associates Jobs (NOW HIRING)

Quality Associate Location: Raleigh, NC Duration: 12 months contract with possible extension Pay rate range: $30/hr-$33/hr Job Summary The Contractor Quality Associate, Biologics will play a key role ...

The Field Quality Associate works on-site at their assigned service location(s) Onboarding Location: Corporate travel to our office in Auburn, IN is required for onboarding and training during your ...

First Shift Sr. Quality Associate I/II: Position Summary: This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information Management System ...

The Field Quality Associate works on-site at their assigned service location(s) Onboarding Location: Corporate travel to our office in Auburn, IN is required for onboarding and training during your ...

Builds, manages, and sustains a team of technical quality associates assigned to product development and in-process quality. * Ability to develop relevant training programs and to instruct the work ...

The Quality Associate will be responsible for performing in-process quality checks and testing, as well as ensuring the Critical Control Points are met throughout the manufacturing process. Perform ...

Trains production and quality associates on use of product and process inspections. * Lead auditing process for assigned production area * Develop audit checklist to validate process adherence. Train ...

The Quality Associate will be responsible for performing in-process quality checks and testing, as well as ensuring the Critical Control Points are met throughout the manufacturing process. Perform ...

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How much do quality associates jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for quality associates in the United States is $26.93, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $31.49 per hour, depending on experience, location, and employer.

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 a keen attention to detail, understanding of quality control processes, and typically a degree in science, engineering, or a related field. Familiarity with statistical process control tools, quality management systems (QMS), and certifications like Six Sigma or ISO 9001 are highly valuable. Strong problem-solving skills, effective communication, and teamwork help you excel in identifying and addressing quality issues. These skills ensure products or services consistently meet standards, which is vital for customer satisfaction and regulatory compliance.

What are some common challenges Quality Associates face when ensuring compliance with industry standards?

Quality Associates often work in fast-paced environments where maintaining compliance with evolving industry standards can be challenging. They must pay close attention to detail while reviewing documentation and conducting product inspections, as even minor oversights can lead to non-compliance. Balancing efficiency with accuracy, especially when production schedules are tight, is another common hurdle. Collaborating with cross-functional teams to resolve issues and implement corrective actions is essential to maintain consistent quality throughout all processes.

What are Quality Associates?

Quality Associates are professionals who assist in maintaining and improving the quality standards of products or services within an organization. Their responsibilities often include inspecting materials, monitoring production processes, conducting tests, and documenting results to ensure compliance with company and regulatory requirements. They work closely with quality engineers and managers to implement quality assurance procedures and help identify areas for process improvement. Quality Associates play a vital role in preventing defects and ensuring customer satisfaction.

What is the difference between Quality Associates vs Quality Inspectors?

AspectQuality AssociatesQuality Inspectors
CertificationsOften requires certifications like ASQ CQE or CQAMay require basic quality or inspection certifications
Work EnvironmentInvolves process analysis, documentation, and quality managementPrimarily focuses on inspecting products and parts
Employer & Industry UsageUsed across manufacturing, healthcare, and service industriesCommonly found in manufacturing and production settings

Quality Associates typically engage in quality management, process improvement, and documentation, often requiring certifications like CQA. Quality Inspectors mainly perform product inspections to ensure quality standards are met. While both roles focus on quality, Quality Associates have broader responsibilities in quality systems, whereas Quality Inspectors concentrate on product verification.

More about Quality Associates jobs

Quality Associate - Raleigh, NC

Kellton Tech

Raleigh, NC • On-site

$30 - $33/hr

Contractor

Posted 25 days ago


Job description

Title: Quality Associate
Location: Raleigh, NC
Duration: 12 months contract with possible extension
Pay rate range: $30/hr-$33/hr
 
Job Summary
The Contractor Quality Associate, Biologics will play a key role in supporting data migration, batch record review, release activities, and building trackers to enhance operational efficiency. This position requires strong attention to detail, familiarity with document management systems such as Veeva Vault, and proficiency in Excel. Experience in Quality Assurance is essential, and knowledge of Power BI is preferred to support data visualization and reporting. The associate will collaborate with cross-functional teams to ensure accurate documentation, timely release of batches, and development of tools to monitor key performance indicators.
The position requires familiarity with Veeva Vault or similar document management systems and Power BI. While Power BI proficiency is preferred, it is not a mandatory requirement for the role.
 
Essential Functions
Lead and manage the migration of quality documents into Veeva Vault, ensuring accuracy and compliance with documentation standards.
Support the transition of legacy records into Veeva, maintaining traceability and completeness.
Build and maintain trackers to monitor key performance indicators (KPIs), batch record status, and release metrics.
Assist in batch record reviews to ensure documentation is complete, compliant, and ready for release.
Support release activities by coordinating documentation readiness and collaborating with QA team members and cross functional teams.
 
Requirements
Education:
Associate degree (required); BS/BA in pertinent life sciences or closely related field (preferred)
Technical:
3+ years of pharmaceutical/biotech working experience in Quality Assurance in an FDA-regulated industry.
Experience with batch record review, document control, and release processes.
Familiarity with SAP inventory system.
Proficient in Microsoft Office tools, and Veeva Quality systems.