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 ...
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 ...
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 ...
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 ...
Senior Quality Engineer - CAPA
Covington, GA · On-site
$75K - $101K/yr
Position Summary The Senior Quality Systems Engineer - CAPA & Continuous Improvement serves as a subject matter expert (SME) for Quality Systems with primary responsibility for the Corrective and ...
Senior Quality Engineer - CAPA
Covington, GA · On-site
$75K - $101K/yr
Position Summary The Senior Quality Systems Engineer - CAPA & Continuous Improvement serves as a subject matter expert (SME) for Quality Systems with primary responsibility for the Corrective and ...
Senior Quality Engineer - CAPA
Covington, GA · On-site
$75K - $101K/yr
Position Summary The Senior Quality Systems Engineer - CAPA & Continuous Improvement serves as a subject matter expert (SME) for Quality Systems with primary responsibility for the Corrective and ...
Senior Quality Engineer - CAPA
Covington, GA · On-site
$75K - $101K/yr
Position Summary The Senior Quality Systems Engineer - CAPA & Continuous Improvement serves as a subject matter expert (SME) for Quality Systems with primary responsibility for the Corrective and ...
Experience with document control and electronic quality management systems preferred * Must be able to pass a background investigation commensurate with position sensitivity designation * Must be ...
Experience with document control and electronic quality management systems preferred * Must be able to pass a background investigation commensurate with position sensitivity designation * Must be ...
Quality Manager
Marietta, GA · On-site
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 ...
Quick apply
Quality Manager
Marietta, GA · On-site
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 Manager
Marietta, GA · On-site
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 Manager
Marietta, GA · On-site
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 Site Leader
Columbus, GA · On-site +1
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 Site Leader
Columbus, GA · On-site +1
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 Site Leader
Columbus, GA · On-site
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 Site Leader
Columbus, GA · On-site
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 Manager
Senoia, GA · On-site
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.
Quality Manager
Senoia, GA · On-site
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Quality Assurance Manager
Albany, GA · On-site
$75K - $100K/yr
Conducting Quality Assurance and Quality Systems training * Aligning quality processes with QMS; supporting reduced inspection schedules with SPC Qualifications: * Bachelor's or Associate degree in a ...
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Quality Assurance Manager
Albany, GA · On-site
$75K - $100K/yr
Conducting Quality Assurance and Quality Systems training * Aligning quality processes with QMS; supporting reduced inspection schedules with SPC Qualifications: * Bachelor's or Associate degree in a ...
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 ...
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 ...
HVAC Cleaning Tech
Norcross, GA · On-site
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 ...
Quick apply
HVAC Cleaning Tech
Norcross, GA · On-site
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 ...
Quality Associate
Ellabell, GA · On-site
$60K/yr
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 ...
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Quality Associate
Ellabell, GA · On-site
$60K/yr
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 ...
Strengthen manufacturing quality systems by improving process capability, first-pass yield, defect reduction, and product reliability. * Lead enterprise root cause analysis, CAPA, risk management ...
Plant Quality Manager
Gainesville, GA · On-site
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 ...
Plant Quality Manager
Gainesville, GA · On-site
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 ...
Plant Quality Manager
Gainesville, GA · On-site
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 ...
Plant Quality Manager
Gainesville, GA · On-site
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 ...
Quality Systems information
See Georgia salary details
$45.6K - $53.3K
8% of jobs
$53.3K - $60.9K
12% of jobs
$63.5K is the 25th percentile. Wages below this are outliers.
$60.9K - $68.6K
17% of jobs
The median wage is $75.5K / yr.
$68.6K - $76.3K
15% of jobs
$76.3K - $84K
12% of jobs
$84K - $91.7K
6% of jobs
$98.9K is the 75th percentile. Wages above this are outliers.
$91.7K - $99.3K
5% of jobs
$99.3K - $107K
6% of jobs
$107K - $114.7K
13% of jobs
$114.7K - $122.4K
3% of jobs
$122.4K - $130K
2% of jobs
$45.6K
$83.3K
$130K
How much do quality systems jobs pay per year?
How does a quality systems professional typically collaborate with other departments to maintain compliance and improve processes?
What are the key skills and qualifications needed to thrive as a quality systems professional, and why are they important?
What is a quality system?
What is the difference between Quality Systems vs Quality Assurance?
| Aspect | Quality Systems | Quality Assurance |
|---|---|---|
| Focus | Developing, implementing, and maintaining quality management systems | Monitoring and verifying product quality through audits and inspections |
| Certifications | ISO 9001, ISO 13485, QS standards | ISO 9001, industry-specific standards |
| Work Environment | Quality departments, compliance teams | Production lines, inspection units |
| Employer Usage | Manufacturers, healthcare, aerospace | Manufacturers, 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.

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.
About Voyant
Sourced by ZipRecruiter
Industry
Software development
Company size
11 - 50 Employees
Headquarters location
Austin, TX, US
Year founded
2006