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Quality Control Associate Jobs in Elgin, SC (NOW HIRING)

MUSC

Medical Laboratory Technician II -PRN

Camden, SC · On-site

MLTs prepare specimens for testing, perform routine laboratory tests, perform quality control and ... Associates degree in Medical Laboratory Technology. Experience: At least one year of clinical ...

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Quality Control Associate information

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$10

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How much do quality control associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for quality control associate in Elgin, SC is $22.77, according to ZipRecruiter salary data. Most workers in this role earn between $16.54 and $27.74 per hour, depending on experience, location, and employer.

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.

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

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 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 cities near Elgin, SC are hiring for Quality Control Associate jobs? Cities near Elgin, SC with the most Quality Control Associate job openings:
Quality Control Associate jobs near you

Operations Visual Inspector Tier I

Nephron Pharmaceuticals

West Columbia, SC • On-site

Full-time

Re-posted 6 days ago

Job description

Job Purpose:
The Production Visual Inspector is responsible for performing visual inspection activities for injectable and ophthalmic pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and promoting a safe and compliant work environment.
Essential Duties and Responsibilities:
• Perform 100% visual inspection of ophthalmic and parenteral drug products, including vials, syringes, ampoules, bottles, and IV bags, in accordance with cGMP requirements and approved inspection procedures
• Inspect products for particulate matter, cosmetic defects, container closure integrity defects, fill level discrepancies, discoloration, cracks, chips, leaks, and other non-conformances
• Execute manual and semi-automated visual inspection activities while maintaining inspection qualification standards and inspection rate requirements
• Maintain compliance with current Good Manufacturing Practices (cGMP), FDA regulations, SOPs, batch records, and data integrity requirements
• Document inspection activities accurately and contemporaneously in batch records, logbooks, and electronic system
• Support line clearance, room setup, and inspection area readiness activities prior to production operations
• Identify, segregate, and report defective or non-conforming materials in accordance with quality procedures
• Participate in initial and annual visual inspection qualification and requalification programs, including defect kit training and certification activities
• Support investigations related to visual defects, deviations, complaints, and non-conforming product event
• Collaborate with Manufacturing, Quality Assurance, and Quality Control teams to ensure product quality and inspection compliance
• Assist with cleaning and sanitization of inspection equipment and work areas in controlled manufacturing environments
• Support continuous improvement initiatives related to inspection processes, defect reduction, and operational efficiency
• Participate in regulatory inspection readiness activities and provide documentation support during audits and inspections
• Follow all safety, gowning, contamination control, and aseptic behavior requirements while working in classified manufacturing environments
Education / Experience:
• High school diploma or GED required; Associate degree or Bachelor's degree in a scientific or technical field preferred
• Experience working with ophthalmic, sterile, injectable, or parenteral products preferred
• Knowledge of cGMP regulations, GDP documentation practices, and FDA pharmaceutical manufacturing requirements preferred
• Ability to identify visual defects and maintain visual acuity and visual inspection qualification standards required
• Experience working in controlled manufacturing environments preferred
• Strong attention to detail, manual dexterity, and ability to maintain concentration during repetitive inspection activities required
Working Conditions / Physical Requirements:
• Position requires bending (desk to floor), lifting (up to 15 lbs.), corrected vision (20/20), standing, sitting, typing, and walking.
• Ability to maintain concentration during repetitive inspection activities required.

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