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Quality Inspector Jobs in Toccoa, GA (NOW HIRING)

Quality Tech I

Westminster, SC · On-site

$16 - $21.50/hr

The Quality Technician is responsible for maintaining and administering gauge validation and supporting the calibration system. The Quality Technician is also responsible for performing system and ...

Quality Technician II

Westminster, SC · On-site

$16 - $21.50/hr

The Quality Technician II is responsible for maintaining and administering gauge validation and supporting the calibration system. The Quality Technician II is also responsible for performing system ...

Title: QA Technician, 1st Shift Req ID: 6038 City, State: Hartwell, GA, Georgia (US-GA) Classification: Nonexempt Recruiter: Jennifer Berry Fleming Title: QA TECHNICIAN, 1st Shift City, State:

QA Technician,1st ShiftReq ID:6038City, State:Hartwell, GA, Georgia (US-GA)Classification:NonexemptRecruiter:Jennifer Berry FlemingTitle:QA TECHNICIAN, 1st ShiftCity, State:Hartwell, GaReports to:

Title: QA Technician, 1st Shift Req ID: 6038 City, State: Hartwell, GA, Georgia (US-GA) Classification: Nonexempt Recruiter: Jennifer Berry Fleming Title: QA TECHNICIAN, 1st Shift City, State:

Showing results 41-60

Quality Inspector information

See Toccoa, GA salary details

$9

$16

$25

How much do quality inspector jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for quality inspector in Toccoa, GA is $16.00, according to ZipRecruiter salary data. Most workers in this role earn between $12.64 and $18.12 per hour, depending on experience, location, and employer.

What is the difference between Quality Inspector vs Quality Control Technician?

AspectQuality InspectorQuality Control Technician
CertificationsISO 9001, ASQ certificationsISO 9001, ASQ certifications
Work EnvironmentManufacturing plants, labsManufacturing facilities, labs
Employer & Industry UsageManufacturing, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Primary FocusInspecting products for defects, ensuring standardsPerforming tests, measuring quality parameters

Both roles involve quality assurance in manufacturing settings and often require similar certifications. However, Quality Inspectors primarily focus on visual and dimensional inspection of products, while Quality Control Technicians perform testing and measurements to verify quality standards. Understanding these differences helps employers and job seekers identify the right role based on skills and responsibilities.

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

To thrive as a Quality Inspector, you need strong attention to detail, knowledge of quality standards, and experience with inspection techniques, often supported by a high school diploma or technical certification. Familiarity with measurement tools such as calipers, micrometers, and quality management systems (QMS) like ISO 9001 is essential. Excellent problem-solving skills, effective communication, and a commitment to teamwork are valuable soft skills in this role. These qualifications ensure products consistently meet safety and regulatory standards, minimizing defects and supporting operational excellence.

How much do quality inspectors earn?

Quality inspectors typically earn between $35,000 and $60,000 annually, depending on experience, industry, and location. Entry-level inspectors may start at lower wages, while those with specialized skills or certifications can earn higher salaries. Many inspectors work full-time, often in manufacturing, construction, or healthcare environments, and may require knowledge of inspection tools and standards.

What does a quality inspector do?

A Quality Inspector is responsible for examining products and materials for defects or deviations from specifications. They use various measuring tools and testing procedures to ensure that items meet required quality standards before they reach customers. Quality Inspectors document their findings, report issues to supervisors, and may recommend improvements to production processes. Their role is essential in maintaining product safety, reliability, and customer satisfaction.

How does a quality inspector typically collaborate with production and engineering teams to resolve quality issues?

Quality Inspectors work closely with production and engineering teams to identify, document, and address quality concerns as they arise. When an issue is detected, inspectors provide detailed reports and may participate in root cause analysis meetings with engineers and production supervisors. Their insights help implement corrective actions and prevent recurrence, ensuring that all products meet the required standards. This collaborative environment promotes continuous improvement and fosters strong communication between departments.

What is the work of a quality inspector?

A quality inspector examines products or materials to ensure they meet specified standards and quality requirements. They perform inspections using tools like calipers or gauges, document findings, and may recommend corrective actions to prevent defects. This role often requires attention to detail and knowledge of quality control procedures and standards.
More about Quality Inspector jobs
What cities near Toccoa, GA are hiring for Quality Inspector jobs? Cities near Toccoa, GA with the most Quality Inspector job openings:
Infographic showing various Quality Inspector job openings in Toccoa, GA as of August 2026, with employment types broken down into 82% Full Time, 9% Contract, and 9% Nights. Highlights an 100% In-person job distribution, with an average salary of $33,289 per year, or $16 per hour.

Quality Assurance Specialist - Complaints NOT REMOTE IN GA

Pharma Tech Services LLC

Royston, GA • On-site

Full-time

Re-posted 8 days ago


Job description

Description:

· Receive, log, and track product complaints in compliance with customer quality agreements, internal procedures, and regulatory requirements.

· Assist in evaluating complaints for potential quality, safety, or regulatory impact.

· Support investigations into product complaints by gathering data, reviewing batch records, and coordinating with Manufacturing, Quality Control, and other departments.

· Document complaint investigations in accordance with GDP and ALCOA+ principles, ensuring accuracy and completeness.

· Escalate critical or serious complaints to QA management as appropriate.

· Support trending and analysis of complaint data; assist in identifying potential issues and recommending improvements.

· Participate in preparation for regulatory inspections, customer audits, and internal audits related to complaint management.

· Assist in revising or drafting SOPs, work instructions, and QA procedures related to complaint handling.

· Collaborate with QA and cross-functional colleagues to ensure timely closure of complaint investigations.

· Initiate SCARs, when deemed necessary, for non-conforming materials discovered in the manufacturing process.

· Coordinate cross-functionally with Procurement, Operations, and Quality teams to drive closure of SCARs and ensure supplier accountability.

· Maintain product retention samples in clean and organized Retain Room(s) that are compliant with all internal procedures and regulatory requirements.

· Discard product retention samples, as needed, with appropriate documentation following all regulatory requirements.

· Maintain audit readiness and compliance with FDA, EMA, ICH, and other regulatory expectations.

· All other activities commensurate with the role, as required

Requirements:Minimum Qualifications
  • Bachelor’s degree in a relevant scientific discipline (e.g., Chemistry, Biology, Microbiology, Pharmaceutical Sciences) or equivalent combination of education and experience
  • Minimum of 2–4 years of experience in Quality Assurance within a GMP-regulated environment (pharmaceutical preferred)
  • Demonstrated experience handling product complaints, investigations, or deviations
  • Working knowledge of 21 CFR Parts 210 and 211 and applicable FDA guidance
  • Proficiency in quality systems (e.g., TrackWise, MasterControl, or equivalent electronic QMS)
  • Strong technical writing and documentation skills
Core Competencies
  • Thorough understanding of Good Manufacturing Practices (GMP) and data integrity principles (ALCOA+)
  • Ability to conduct root cause analysis (e.g., 5 Whys, Fishbone, CAPA methodologies)
  • Strong attention to detail with the ability to identify trends and systemic issues
  • Effective cross-functional communication (Operations, QC, Regulatory Affairs, Customer Service)
  • Ability to manage multiple investigations simultaneously while meeting regulatory timelines
  • Critical thinking and decision-making in a regulated environment
Regulatory & Compliance Requirements
  • Ensure all complaint handling activities comply with 21 CFR Part 211, specifically Subpart J – Records and Reports (Complaint Files)
  • Maintain complaint files in accordance with FDA data integrity expectations and internal SOPs
  • Support FDA inspections, audits, and regulatory inquiries related to complaint handling
  • Ensure timely reporting of adverse events, product quality complaints, and potential reportable events (e.g., Field Alerts, if applicable)