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Quality Systems Jobs in Georgia (NOW HIRING)

This role will own the quality system framework, supplier quality oversight, CAPA administration, audit readiness, and regulatory support activities, while working cross-functionally with Operations ...

QUALITY SYSTEMS OVERSIGHT Develop, implement, and maintain site-specific quality systems and ensure they are aligned with corporate standards and regulatory requirements. * REGULATORY AUDITS ...

QUALITY SYSTEMS OVERSIGHT Develop, implement, and maintain site-specific quality systems and ensure they are aligned with corporate standards and regulatory requirements. * REGULATORY AUDITS ...

Quality Systems, Compliance & Food Safety * Lead and maintain the site Quality Management System (QMS), ensuring compliance with ISO 9001, SQF/BRCGS, customer requirements, and regulatory standards.

Conduct quality systems gap analyses at key manufacturing sites and implement tailored solutions. * Serve as the escalation point and leader for quality issues, including product withdrawals and ...

Since 1986 Air Quality Systems has provided residential, commercial and industrial HVAC system cleanings in Norcross and surrounding areas. We are a member of the National Air Duct Cleaners ...

Collect, organize, and input inspection data into quality management systems. * Support calibration and maintenance of inspection tools and equipment. * Prepare and maintain quality records, reports ...

Strengthen manufacturing quality systems by improving process capability, first-pass yield, defect reduction, and product reliability. * Lead enterprise root cause analysis, CAPA, risk management ...

Establish and improve quality systems, prevent defects, and drive root cause analysis, corrective actions, and containment of major issues. Drive Cross-Functional Alignment * Act as the primary ...

Establish and improve quality systems, prevent defects, and drive root cause analysis, corrective actions, and containment of major issues. Drive Cross-Functional Alignment * Act as the primary ...

Showing results 41-60

Quality Systems information

See Georgia salary details

$45.6K

$83.3K

$130K

How much do quality systems jobs pay per year?

As of Aug 11, 2026, the average yearly pay for quality systems in Georgia is $83,267.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,800.00 and $103,400.00 per year, depending on experience, location, and employer.

How does a quality systems professional typically collaborate with other departments to maintain compliance and improve processes?

Quality Systems professionals work closely with departments like Manufacturing, Regulatory Affairs, and Research & Development to ensure that quality standards and compliance requirements are consistently met. They facilitate communication between teams, conduct audits, and coordinate corrective actions to address any issues. Collaboration often involves leading training sessions, reviewing documentation, and implementing continuous improvement initiatives based on feedback from various stakeholders. This cross-functional teamwork is essential for maintaining certifications and driving process excellence throughout the organization.

What are the key skills and qualifications needed to thrive as a quality systems professional, and why are they important?

To thrive as a Quality Systems professional, a solid understanding of quality management principles, process improvement methodologies, and compliance standards such as ISO 9001 is essential, often supported by a relevant degree or certification. Familiarity with quality management software (QMS), audit tools, and document control systems is typically required. Strong attention to detail, problem-solving abilities, and effective communication are vital soft skills that distinguish top performers in this role. These capabilities are crucial for maintaining regulatory compliance, driving continuous improvement, and ensuring consistent product or service quality.

What is a quality system?

Quality Systems are structured processes and procedures that organizations establish to ensure their products or services consistently meet defined quality standards and regulatory requirements. These systems typically include documentation, training, auditing, corrective actions, and continuous improvement practices. Quality Systems are essential in industries like manufacturing, pharmaceuticals, and healthcare to maintain compliance and customer satisfaction. Implementing a robust Quality System helps organizations minimize errors, improve efficiency, and comply with industry regulations.

What is the difference between Quality Systems vs Quality Assurance?

AspectQuality SystemsQuality Assurance
FocusDeveloping, implementing, and maintaining quality management systemsMonitoring and verifying product quality through audits and inspections
CertificationsISO 9001, ISO 13485, QS standardsISO 9001, industry-specific standards
Work EnvironmentQuality departments, compliance teamsProduction lines, inspection units
Employer UsageManufacturers, healthcare, aerospaceManufacturers, service providers

While both roles aim to ensure product quality, Quality Systems focuses on establishing and maintaining the overall quality management framework, whereas Quality Assurance emphasizes verifying and validating that products meet quality standards through testing and inspections.

What are the most commonly searched types of Quality Systems jobs in Georgia? The most popular types of Quality Systems jobs in Georgia are:
What are popular job titles related to Quality Systems jobs in Georgia? For Quality Systems jobs in Georgia, the most frequently searched job titles are:
What cities in Georgia are hiring for Quality Systems jobs? Cities in Georgia with the most Quality Systems job openings:
Infographic showing various Quality Systems job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $83,267 per year, or $40 per hour.

Quality (Plant) - Engineer, Hygiene Systems & Validation

voyant

Gainesville, GA • On-site

Full-time

Re-posted 3 days ago


Job description

Voyant Beauty believes our people are more than just employees; they’re the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual’s contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team.

Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life.

Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel.

If you’re seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey.


A Brief Overview
The Hygiene Systems & Validation Engineer leads the site validation and contamination control strategy to ensure compliance with cGMP regulations and company quality standards. This role serves as the subject matter expert (SME) for hygiene systems and validation, driving continuous improvement and standardization across validation programs. This position is responsible for planning, executing, and overseeing validation activities including process, cleaning, equipment, and utility system qualifications for OTC products, cosmetics, and regulated systems. The Engineer, Validation Technical partners closely with Engineering, Quality Assurance, and Operations to ensure validation and hygiene programs meet regulatory and internal requirements. The role also owns audit readiness and supports regulatory inspections, while proactively mitigating contamination risks across the site.
What you will do

  • Lead the validation lifecycle strategy for new equipment, manufacturing processes, and facility changes, including development, standardization, and approval of IQ/OQ/PQ protocols and final reports.
  • Define, implement, and continuously improve site-wide contamination control programs, including cleaning validation, environmental monitoring, and critical utility systems (e.g., USP water, compressed air).
  • Own audit readiness for validation and hygiene systems, serving as the primary SME during internal and external audits and regulatory inspections.
  • Develop, review, and maintain SOPs, validation protocols, and technical documentation to ensure compliance, consistency, and inspection readiness.
  • Provide technical leadership and cross-functional support to Engineering, Quality, and Operations on validation, hygiene, and compliance-related initiatives.
  • Mentor and provide guidance to junior engineers and technicians, supporting development of validation and quality capabilities across the site.
  • Lead environmental monitoring oversight and interface with third-party laboratories; evaluate microbial and analytical data to assess risk and ensure program effectiveness.
  • Provide input into equipment design and purchase decisions with validation and compliance requirements in mind
  • Support quality investigations, deviations, and CAPA related to validation or equipment failures
  • Drive continuous improvement initiatives across validation and contamination control programs
  • Remain current with regulatory guidance, industry best practices, and emerging risks in cGMP environments
  • Some duties may vary slightly by location


Education Qualifications

  • Bachelor's Degree Mechanical Engineering, Chemical Engineering, or related technical field (Required)


Experience Qualifications

  • 4-6 years Validation experience within a cGMP manufacturing environment (OTC, pharmaceutical, cosmetics, or personal care) (Required)
  • 4-6 years Cross-functional project leadership across engineering, quality, and operations (Required)
  • 4-6 years FDA/OTC regulated environments (Preferred)
  • 4-6 years Leading audits, inspections, and regulatory interactions (Preferred)


Skills and Abilities

  • Process, cleaning, equipment, and utility validation (High proficiency)
  • IQ/OQ/PQ protocol development and execution (High proficiency)
  • cGMP compliance and regulatory standards (High proficiency)
  • Regulatory inspection leadership (FDA and customer audits) (High proficiency)
  • Risk-based validation strategy and decision making (High proficiency)
  • Contamination control program ownership (cleaning, EM, utilities) (High proficiency)
  • SOP and technical document development (High proficiency)
  • Cross-functional collaboration and stakeholder influence (High proficiency)
  • Influencing without authority across functions (High proficiency)
  • Project leadership and prioritization across multiple initiatives (High proficiency)
  • Root cause analysis and deviation/CAPA support (Medium proficiency)
  • Environmental monitoring and lab coordination (Medium proficiency)
  • Analytical and microbiological test interpretation (Medium proficiency)


Licenses and Certifications

  • Lean Six Sigma certification or equivalent training (Preferred)

To Staffing and Recruiting Agencies: Our company does not accept unsolicited curriculum vitae’s or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae’s or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae’s or application.

Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.