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Quality Associate Jobs in Charleston, SC (NOW HIRING)

Thorne

Quality Associate 1

Summerville, SC · On-site

The Quality Associate I supports Thorne's Quality Management System (QMS) by assisting with quality processes, documentation, and compliance activities that help ensure products consistently meet ...

Thorne

Quality Control Data Associate

Summerville, SC · On-site

Quality Control Data Associate Department: Lab Employment Type: Full Time Location: Summerville, SC Description At Thorne, we work to deliver high-quality, science-backed solutions to empower ...

LaBine and Associates

Quality Engineer

Charleston, SC

$68K - $88K/yr

Our client is seeking a Quality Engineer for their Charleston, South Carolina facility. You will be a part of a globally recognized company that offers technologically innovative solutions for ...

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All JobsQuality Associate JobsQuality Associate Jobs in Charleston, SC

Quality Associate information

See Charleston, SC salary details

$10

$25

$47

How much do quality associate jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for quality associate in Charleston, SC is $25.20, 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 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 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.

More about Quality Associate jobs
What are the most commonly searched types of Quality jobs in Charleston, SC? The most popular types of Quality jobs in Charleston, SC are:
What are popular job titles related to Quality Associate jobs in Charleston, SC? For Quality Associate jobs in Charleston, SC, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Charleston, SC look for? The top searched job categories for Quality Associate jobs in Charleston, SC are:
What cities near Charleston, SC are hiring for Quality Associate jobs? Cities near Charleston, SC with the most Quality Associate job openings:
Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Charleston, SC as of June 2026, with employment types broken down into 2% As Needed, 59% Full Time, 31% Part Time, 1% Temporary, and 7% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $52,423 per year, or $25.2 per hour.

Quality Associate 1

Thorne

Summerville, SC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Job description

At Thorne, we work to deliver high-quality, science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. At Thorne, you'll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage.

The Quality Associate I supports Thorne's Quality Management System (QMS) by assisting with quality processes, documentation, and compliance activities that help ensure products consistently meet company, customer, and regulatory requirements. This role provides operational support for key quality systems, including product certifications, Change Control, Corrective and Preventive Actions (CAPA), deviations, customer complaints, nonconforming materials, and document control.

Working closely with Quality, Operations, Regulatory Affairs, Product Development, and Supply Chain, the Quality Associate I develops a strong foundation in quality systems while contributing to continuous improvement initiatives and daily quality operations. The ideal candidate is detail-oriented, highly organized, and eager to learn within a regulated manufacturing environment while building expertise in GMP requirements and quality management processes.
  • Support the administration of Thorne's Quality Management System (QMS), including Change Control, Corrective and Preventive Actions (CAPA), Deviations, Nonconforming Materials (NCM), customer complaints, and document control activities.
  • Assist in coordinating third-party product certification activities by gathering documentation and communicating with certification bodies, contract manufacturers, and internal stakeholders.
  • Support the stability program by coordinating sample submissions, maintaining documentation, and assisting with stability data collection and reporting.
  • Assist with customer complaint investigations by collecting information, documenting findings, and supporting timely resolution.
  • Maintain, organize, and update quality documentation, including Standard Operating Procedures (SOPs), controlled forms, and quality records.
  • Participate in internal audits and inspections while supporting audit preparation and follow-up activities.
  • Assist in reviewing new products, processes, and documentation to help ensure compliance with GMP requirements and internal quality standards.
  • Generate routine quality reports, KPI metrics, and status updates to support quality system monitoring.
  • Complete ERP and ETQ transactions related to quality processes and maintain accurate electronic records.
  • Collaborate with cross-functional teams to support quality initiatives and continuous improvement efforts.
  • Maintain compliance with GMP, FDA, OSHA, and all applicable company policies and regulatory requirements.
  • Escalate quality concerns or potential compliance issues to appropriate team members and support timely resolution.
  • Perform other duties as assigned.

Education & Experience 
  • High school diploma or GED required; Associate's or Bachelor's degree in a scientific discipline, Quality, Manufacturing, or a related field preferred.
  • 0-2 years of experience in Quality Assurance, Manufacturing, Laboratory Operations, Regulatory Affairs, or a related field preferred.
  • Internship, co-op, or experience within a GMP-regulated manufacturing environment is a plus.
  • Familiarity with quality management systems or regulated manufacturing environments is preferred.
Technical Knowledge 
  • Basic understanding of Good Manufacturing Practices (GMP) and quality system principles.
  • Ability to interpret Standard Operating Procedures (SOPs), work instructions, and technical documentation.
  • Proficiency with Microsoft Office Suite and willingness to learn ERP and electronic Quality Management Systems (eQMS), such as ETQ.
  • Ability to prepare accurate documentation, reports, and quality records.
Core Competencies 
  • Strong attention to detail and commitment to accuracy.
  • Excellent organizational and time management skills with the ability to prioritize multiple assignments.
  • Strong verbal and written communication skills.
  • Ability to work collaboratively in a cross-functional team environment while developing independent decision-making skills.
  • Demonstrated initiative, curiosity, and a willingness to learn new quality systems and regulatory requirements.
  • Analytical problem-solving skills with the ability to recognize and escalate quality concerns appropriately.
  • Adaptability and a commitment to continuous improvement in a fast-paced manufacturing environment.
  • Competitive compensation
  • 100% company-paid medical, dental, and vision insurance coverage for employees
  • Company-paid short- and long-term disability insurance
  • Company- paid life insurance
  • 401k plan with employer matching contributions up to 4%
  • Gym membership reimbursement
  • Monthly allowance of Thorne supplements
  • Paid time off, volunteer time off and holiday leave
  • Training, professional development, and career growth opportunities

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