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Quality Control Jobs in Gaston, SC (NOW HIRING)

Shortage Control Lead - Full-Time

Columbia, SC · On-site

$14/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As a Shortage Control Lead you will be responsible for mitigating theft and fraud in high shortage areas of the store while promoting a safe and secure store environment. You will engage with our ...

PC Inspector

Columbia, SC · On-site

$23.03/hr

Responsible for QC sampling (retains, nova septum and QC laboratories) * Verification and release of BFS code magazine * Perform resin verification * Maintain/ Review batch record documentation of ...

PC Inspector

Columbia, SC · On-site

$23.03/hr

Responsible for QC sampling (retains, nova septum and QC laboratories) * Verification and release of BFS code magazine * Perform resin verification * Maintain/ Review batch record documentation of ...

Be Seen First

Familiar with punch list writing or general QC/QA principles. * Home Renovation or Remodeling * Familiar with fit and finish reviews or warranty walk through with homeowners Ideal candidates will be:

New

... control measures. - Documenting audit findings and providing actionable recommendations to enhance quality performance. - Assisting in the development and maintenance of quality assurance policies ...

... control measures. - Documenting audit findings and providing actionable recommendations to enhance quality performance. - Assisting in the development and maintenance of quality assurance policies ...

Quality Inspector, EI&C

Columbia, SC · On-site

$49 - $58/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Conduct regularly scheduled QA/QC meetings, review logs of Deficiencies, Punch List, and other items required and maintain documentation and meeting minutes within job folder * Prepare reports on ...

Director, Supplier Quality

Columbia, SC · On-site

$180 - $220/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead all supplier quality planning and execution of manufacturing, assembly techniques and quality control processes from the advanced development phase to serial production * Lead and oversee all ...

Director, Supplier Quality

Columbia, SC · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead all supplier quality planning and execution of manufacturing, assembly techniques and quality control processes from the advanced development phase to serial production * Lead and oversee all ...

Plumbing Quality Inspector

Lexington, SC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Previous experience in home inspections or quality control, especially in construction or plumbing, is highly valued * A thorough knowledge of local, state, and national plumbing codes is crucial for ...

Quality Supervisor

Columbia, SC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assigns employees to maximize quality control goals. * Ensures that directed shift staffing levels are maintained. * Hires quality auditors for shift. * Interfaces with HR for employee issues.

Showing results 21-40

Quality Control information

See Gaston, SC salary details

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How much do quality control jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for quality control in Gaston, SC is $20.46, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $22.88 per hour, depending on experience, location, and employer.

What is the job of quality control?

The job of quality control involves inspecting products or services to ensure they meet specified standards and are free of defects. Quality control professionals use testing, measurements, and documentation to identify issues and improve processes, often working with tools like checklists and quality management systems. Strong attention to detail and knowledge of industry standards are essential for this role.

What is the difference between Quality Control vs Quality Assurance?

AspectQuality ControlQuality Assurance
FocusDetecting defects in products or servicesPreventing defects through process improvements
ActivitiesInspections, testing, samplingProcess audits, standards development
CredentialsOften requires technical training or certifications in testingCertifications like ISO, Six Sigma are common
Work EnvironmentLaboratory, production lines, manufacturingProcess development, documentation, audits

While Quality Control focuses on identifying defects after production, Quality Assurance aims to prevent defects through process improvements. Both roles are essential for maintaining product quality, but they differ in approach and activities.

Do you need a degree for quality control?

A degree is not always required for a quality control position, as many employers accept candidates with a high school diploma or equivalent. However, having post-secondary education or certifications in quality management, such as Six Sigma or ISO standards, can improve job prospects and advancement opportunities.

Is quality control a good career choice?

Quality control is a viable career that involves inspecting products and processes to ensure standards are met, often requiring attention to detail and knowledge of industry regulations. It can offer stable employment with opportunities for advancement and may require certifications or training in specific tools or standards. The field is important across many industries, including manufacturing, healthcare, and food production.

What is quality control?

Quality control (QC) is a process by which businesses ensure that their products or services meet specific standards of quality. This typically involves systematic inspection, testing, and corrective actions to detect and address defects or inconsistencies. Quality control helps maintain customer satisfaction, comply with regulations, and reduce waste or costly errors. QC can be applied at various stages of production and is essential in industries such as manufacturing, food production, and pharmaceuticals.

What are some common challenges faced by quality control professionals and how can they be addressed?

Quality Control professionals often encounter challenges such as maintaining consistency across production batches, adapting to new regulatory standards, and managing tight deadlines without compromising quality. Addressing these challenges requires strong attention to detail, effective communication with production and engineering teams, and continuous learning to stay updated on industry best practices. Many companies support their QC staff with regular training sessions, clear documentation protocols, and collaborative problem-solving meetings to ensure quality standards are upheld.

Is quality control a good career path?

Quality control is a viable career that involves inspecting products and processes to ensure standards are met, often requiring attention to detail and knowledge of industry regulations. It can lead to advancement into supervisory or specialized roles and may require certifications such as Six Sigma or ISO standards. The job typically offers stable employment in manufacturing, healthcare, or technology sectors.

What are the key skills and qualifications needed to thrive as a quality control professional?

To thrive as a Quality Control professional, you need keen attention to detail, analytical skills, and a background in science, engineering, or manufacturing, often supported by relevant certifications like Six Sigma or ISO standards. Familiarity with quality management systems (QMS), statistical process control (SPC) software, and inspection equipment is typically required. Strong problem-solving abilities, communication, and teamwork set top performers apart in this role. These skills are crucial to ensure product consistency, prevent defects, and maintain compliance with industry standards.
What are the most commonly searched types of Quality Control jobs in Gaston, SC? The most popular types of Quality Control jobs in Gaston, SC are:
What cities near Gaston, SC are hiring for Quality Control jobs? Cities near Gaston, SC with the most Quality Control job openings:
Infographic showing various Quality Control job openings in Gaston, SC as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $42,551 per year, or $20.5 per hour.

Microbiology Quality Investigator

Nephron Pharmaceuticals

West Columbia, SC • On-site

$23.25 - $30.50/hr

Full-time

Re-posted 13 days ago


Job description

Job Purpose:
Microbiology Quality Investigators ensure compliance with FDA regulations in the areas of microbiology-related investigations. Microbiology Quality Investigators are responsible for ensuring the Microbiology department's adherence to FDA regulations. This involves completion of non-conformance investigations, the drafting of pertinent memorandums, managing deviations, and implementing robust corrective and preventive actions (CAPAs). A key aspect of the role is effective inter-departmental collaboration to facilitate the timely completion of all projects. Furthermore, investigators must skillfully manage their individual workload and adapt to shifting priorities to meet departmental and company demands.
Essential Duties and Responsibilities:
  • Effectively completes microbiology excursion reports and associated documentation per procedure within specified timelines.
  • Executes timely completion of CAPAs, Quality Events (QE), memorandums, and deviations as they pertain to the Microbiology program.
  • Coordinates with all areas of Microbiology and other departments to ensure training related to Microbiology excursions and investigations are completed based on findings and associated root cause(s).
  • Understands Microbiology-related guidance, including but not limited to USP, FDA, and compendial standards.
  • Prepares reports and data for EM tracking and trending, as well as tracking and reporting excursions, QEs, and CAPAs.
  • Updates and maintains the investigations electronic logs for visibility.
  • Coordinates with impacted departments and Quality Investigations department to ensure oversight of CAPA plans, investigation outcomes, and reduce future events.
  • Maintains adherence to established Standard Operating Procedures (SOPs) and work instructions.
  • Completes Microbiology SOP revisions.
  • Communicates all Microbiology-related observations, issues, problems, discrepancies, and any violations of company policies or procedures to the Microbiology Investigations Manager, Assistant Director and Director of Microbiology, and VP of Microbiology.

Supplemental Functions:
• Copying, filing, and scanning of investigation-related documents.
  • Knowledgeable in Adobe Acrobat (PDF) advanced features and workflows.
  • Performs other similar duties as required.

Requirements
Knowledge & Skills:
  • Technical background preferred, with knowledge of cGMP, and FDA regulations.
  • 1-3 years of experience with Microsoft Word, Excel, and PowerPoint preferred.
  • Strong writing and organizational skills: experience with technical writing, Root Cause Analysis, and managing multiple projects/assignments simultaneously.
  • Strong understanding of document control procedures, standards, and best practices
  • Familiar with document management software, including Sharepoint and TrackWise software.
  • Effective time management skills including prioritizing and scheduling, as well as the ability to meet all deadlines and manage time effectively.
  • Effective communication and interpersonal abilities to work with cross-functional, fast-paced teams.
  • Familiar with relevant industry regulations and compliance standards.
  • Discretion in handling sensitive and confidential information.
  • Strong critical thinking, analytical, problem-solving, and interpersonal skills.
  • The ability and willingness to change direction and focus to meet shifting organizational and business demands.
  • The ability to manage a multitude of resources and to be accurate and current with data and information.

Education/Experience:
  • Bachelor's degree preferred with 1-2 years of pharmaceutical experience in Quality systems or Microbiology.
  • 1-3 years of experience with MS Word, Excel, and Powerpoint.
  • Pharmaceutical technical writing experience, preferred.

Working Conditions / Physical Requirements:
  • This position requires bending, typing, lifting (up to 40 1bs.), standing, sitting and walking throughout the facility.