Top 79 Quality assurance Jobs in Hartwell, Ga

Quality Assurance Specialist - Complaints NOT REMOTE IN GA
Pharma Tech Services LLC —Royston, GA
- Full-time
- Mid-level
- Bachelor's degree
- In-person
Quality Assurance Specialist In Georgia NOT remote
PTI Georgia LLC —Royston, GA
- Full-time
- Computer literacy
- Mid-level
- Continuous improvement
Factory Quality Specialist (Systems)
Nestlé Purina —Hartwell, GA
- $67,820 - $98,150 a year
- Mid-level
- High school diploma or GED
- Experience equivalent to degree accepted
- Health insurance
- 401(k) matching
Quality Assurance Tester
Avani Technology Solutions Inc —Clemson, SC
- Contract
- Mid-level
- Communication skills
Quick Apply
Quality Analyst
Mach10 Solutions —Comer, GA
- $31.97 - $38.61 an hour
- Full-time
- Mid-level
Quick Apply
3d
Quality Engineer
Mollertech South LLC —Elberton, GA
- $65,000 - $75,000 a year
- Weekends as needed
- 5 years
- Writing skills
- Office
- Health savings account
- Health insurance
Quick Apply
Quality Engineer
Zing Recruiting —Elberton, GA
- $75,000 - $85,000 a year
- Engineering
- Mid-level
- 3 years
- Disability insurance
- Health insurance
Quick Apply
12d
Coding Quality Auditor
Houston Methodist —Georgia
- Full-time
- Anatomy knowledge
- English
- Mid-level
Coding Quality Auditor
Houston Methodist —Georgia
- Full-time
- Anatomy knowledge
- English
- Mid-level
2d
Quality Technician
nVent —Eastanollee, GA
- Full-time
- Bachelor of Science
- Research
- Mid-level
- Employee stock purchase plan
- Disability insurance
QA Technician
Brakebush Brothers, Inc. —Hartwell, GA
- Overtime
- Ability to walk for extended periods
- Computer literacy
- Writing skills
Quality Technician- 1st shift
Vertiv —Anderson, SC
- Microsoft Word
- Microsoft Excel
- Mid-level
Quality & Food Safety Assistant (2nd Shift)
BHJ USA LLC —Hartwell, GA
- Full-time
- Pass drug screening
- US work authorization
- Entry level
Quick Apply
Quality engineer
Mach10 Solutions —Danielsville, GA
- $31.97 - $42.31 an hour
- Full-time
- Mid-level
- Continuous improvement
- Communication skills
Quick Apply
3d
Quality Control Tech
Smurfit Westrock —Anderson, SC
- Overtime
- Computer literacy
- Basic math
- Mid-level
- Health savings account
- AD&D insurance
5d
Lab Technician
Perdue Farms Inc —Bowersville, GA
- Writing skills
- Mid-level
- High school diploma or GED
Supplier Quality Development Manager
BorgWarner —Seneca, SC
- $125,600 - $172,700 a year
- Full-time
- 7 years
- Microsoft Excel
- Up to 50% travel
Quality Engineer
McLaughlin Body Company, Inc. —Anderson, SC
- Full-time
- Mid-level
- 3 years
Quick Apply
6d
Quality Control Inspector
Schneider Electric —Seneca, SC
- Online Application
- Mid-level
- High school diploma or GED
- In-person
- Dental insurance
- Military leave
2d
Plant Sr. Quality Leader
Kroger —Anderson, SC
- Full-time
- Experience working with individuals with disabilities
- Adults
- Analysis skills
Quick Apply

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Quality Assurance Specialist - Complaints NOT REMOTE IN GA

Pharma Tech Services LLC
Royston, GA

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Job Details

Full-time

Qualifications

Content creation for technical audiences
Investigations regulatory compliance
Drug regulation
Technical writing experience within manufacturing
Internal investigations
FDA regulations
Pharmaceutical manufacturing facility experience

Full 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)

Apply Now

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quality assurance jobs in hartwell, ga

Quality Assurance Specialist - Complaints NOT REMOTE IN GA

Quality Assurance Specialist In Georgia NOT remote

Factory Quality Specialist (Systems)

Quality Assurance Tester

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Quality Engineer

Coding Quality Auditor

Coding Quality Auditor

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Lab Technician

Supplier Quality Development Manager

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Quality Control Inspector

Plant Sr. Quality Leader

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