Maintain, improve, and standardize the QMS in alignment with ISO 13485 and customer regulatory requirements * Lead continuous improvement initiatives focused on risk reduction, process capability ...
Maintain, improve, and standardize the QMS in alignment with ISO 13485 and customer regulatory requirements * Lead continuous improvement initiatives focused on risk reduction, process capability ...
Quality Assurance Manager
Milwaukee, WI · On-site
The QA manager will foster culture of continuous improvement within the organization and an ... Oversee the continuous improvement of QMS processes, including documentation, supplier ...
Quality Assurance Manager
Milwaukee, WI · On-site
The QA manager will foster culture of continuous improvement within the organization and an ... Oversee the continuous improvement of QMS processes, including documentation, supplier ...
The QA manager will foster culture of continuous improvement within the organization and an ... Oversee the continuous improvement of QMS processes, including documentation, supplier ...
The QA manager will foster culture of continuous improvement within the organization and an ... Oversee the continuous improvement of QMS processes, including documentation, supplier ...
QMS Quality Engineer - $5,000.00 Sign On Bonus
Cudahy, WI · On-site
$70K - $91K/yr
... with QMS systems, and data analysis, we want to hear from you. This role will offer you the ... You will manage the investigation and resolution process from start to finish, ensuring the issue ...
QMS Quality Engineer - $5,000.00 Sign On Bonus
Cudahy, WI · On-site
$70K - $91K/yr
... with QMS systems, and data analysis, we want to hear from you. This role will offer you the ... You will manage the investigation and resolution process from start to finish, ensuring the issue ...
The Quality Systems Engineer is responsible for maintaining, enhancing, and ensuring the effectiveness of the Quality Management System (QMS) in compliance with FSSC 22000, ISO 9001, ISO 13485, and ...
The Quality Systems Engineer is responsible for maintaining, enhancing, and ensuring the effectiveness of the Quality Management System (QMS) in compliance with FSSC 22000, ISO 9001, ISO 13485, and ...
Quality Systems Engineer
Pleasant Prairie, WI · On-site
The Quality Systems Engineer is responsible for maintaining, enhancing, and ensuring the effectiveness of the Quality Management System (QMS) in compliance with FSSC 22000, ISO 9001, ISO 13485, and ...
Quality Systems Engineer
Pleasant Prairie, WI · On-site
The Quality Systems Engineer is responsible for maintaining, enhancing, and ensuring the effectiveness of the Quality Management System (QMS) in compliance with FSSC 22000, ISO 9001, ISO 13485, and ...
Quality & Safety Manager
Pleasant Prairie, WI · On-site
Own the Quality Management System (QMS). * Review and approve testing protocols, sampling plans, and procedures. * Monitor production quality performance and present findings. * Ensure calibration ...
Quality & Safety Manager
Pleasant Prairie, WI · On-site
Own the Quality Management System (QMS). * Review and approve testing protocols, sampling plans, and procedures. * Monitor production quality performance and present findings. * Ensure calibration ...
Quality & Safety Manager
Pleasant Prairie, WI · On-site
Own the Quality Management System (QMS). * Review and approve testing protocols, sampling plans, and procedures. * Monitor production quality performance and present findings. * Ensure calibration ...
Quick apply
Quality & Safety Manager
Pleasant Prairie, WI · On-site
Own the Quality Management System (QMS). * Review and approve testing protocols, sampling plans, and procedures. * Monitor production quality performance and present findings. * Ensure calibration ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Ensure accurate reporting of non-quality costs and QMS performance to the Management Team and key stakeholders * Act as final quality authority (in collaboration with Engineering) for equipment ...
Quality Assurance Specialist
Waukegan, IL · On-site
$60K - $75K/yr
Maintain improve, and standardize the company's Quality Management System (QMS), including procedures, work instructions, and documentation structure * Identify gaps in current processes and ...
Quality Assurance Specialist
Waukegan, IL · On-site
$60K - $75K/yr
Maintain improve, and standardize the company's Quality Management System (QMS), including procedures, work instructions, and documentation structure * Identify gaps in current processes and ...
Quality Assurance Specialist
Waukegan, IL · On-site
$60K - $75K/yr
Maintain improve, and standardize the company's Quality Management System (QMS), including procedures, work instructions, and documentation structure * Identify gaps in current processes and ...
Quick apply
Quality Assurance Specialist
Waukegan, IL · On-site
$60K - $75K/yr
Maintain improve, and standardize the company's Quality Management System (QMS), including procedures, work instructions, and documentation structure * Identify gaps in current processes and ...
Quality Assurance Specialist
Waukegan, IL · On-site
$60K - $75K/yr
Maintain improve, and standardize the company's Quality Management System (QMS), including procedures, work instructions, and documentation structure * Identify gaps in current processes and ...
Quality Assurance Specialist
Waukegan, IL · On-site
$60K - $75K/yr
Maintain improve, and standardize the company's Quality Management System (QMS), including procedures, work instructions, and documentation structure * Identify gaps in current processes and ...
Maintenance Manager
Cudahy, WI · On-site
The individual must also have a working knowledge of QMS procedures, ability to handle external ... Manages and oversees facility specific operations and maintenance processes and procedures. * Plans ...
Maintenance Manager
Cudahy, WI · On-site
The individual must also have a working knowledge of QMS procedures, ability to handle external ... Manages and oversees facility specific operations and maintenance processes and procedures. * Plans ...
Teach and implement QMS at all levels * Manage Gage Calibration Program * Lead and participate in internal corrective actions * Coordinate and Conduct workstation audits * Monitor and update NCR'
New
Teach and implement QMS at all levels * Manage Gage Calibration Program * Lead and participate in internal corrective actions * Coordinate and Conduct workstation audits * Monitor and update NCR'
New
Quality Engineer
$69K - $115K/yr
Participate in monitoring, and advancement of the following QMS focal points:Change Management, CAPA,Deviation Management, Training Management, Documentation Management, Complaints, Field Corrective ...
Quality Engineer
$69K - $115K/yr
Participate in monitoring, and advancement of the following QMS focal points:Change Management, CAPA,Deviation Management, Training Management, Documentation Management, Complaints, Field Corrective ...
Quality Engineer
Milwaukee, WI · On-site
$69K - $115K/yr
Participate in monitoring, and advancement of the following QMS focal points: Change Management, CAPA, Deviation Management, Training Management, Documentation Management, Complaints, Field ...
Quality Engineer
Milwaukee, WI · On-site
$69K - $115K/yr
Participate in monitoring, and advancement of the following QMS focal points: Change Management, CAPA, Deviation Management, Training Management, Documentation Management, Complaints, Field ...
Qms Manager information
See Racine, WI salary details
$22.5K - $33.9K
12% of jobs
$41.4K is the 25th percentile. Wages below this are outliers.
$33.9K - $45.3K
20% of jobs
$45.3K - $56.8K
14% of jobs
The median wage is $60.6K / yr.
$56.8K - $68.2K
13% of jobs
$68.2K - $79.6K
9% of jobs
$79.6K - $91K
5% of jobs
$98.2K is the 75th percentile. Wages above this are outliers.
$91K - $102.5K
4% of jobs
$102.5K - $113.9K
4% of jobs
$113.9K - $125.3K
2% of jobs
$125.3K - $136.7K
0% of jobs
$136.7K - $148.2K
17% of jobs
$22.5K
$80.8K
$148.2K
How much do qms manager jobs pay per year?
What are the key skills and qualifications needed to thrive as a QMS Manager, and why are they important?
How does a QMS Manager typically collaborate with other departments to ensure compliance and continuous improvement?
What are QMS Managers?
What is the difference between Qms Manager vs Quality Assurance Supervisor?
| Aspect | Qms Manager | Quality Assurance Supervisor |
|---|---|---|
| Certifications | ISO 9001 Lead Auditor, CQE | ISO 9001 Lead Auditor, CQE |
| Work Environment | Oversees quality management systems across departments | Supervises quality assurance team and daily testing activities |
| Industry Usage | Used in manufacturing, aerospace, automotive | Common in manufacturing, pharmaceuticals, food industry |
| Primary Focus | Developing, maintaining, and improving QMS | Monitoring product quality and compliance |
The Qms Manager and Quality Assurance Supervisor roles share similar certifications and industry usage, but the Qms Manager focuses on managing the entire quality management system, while the Supervisor concentrates on daily quality assurance activities. Both positions are vital for ensuring product quality and compliance within manufacturing and related industries.

Full-time
Posted 21 days ago
Job description
Job Title: Quality Manager
Department: Quality
FLSA Status: Exempt
Reports To: CEO, North America
Location: Menomonee Falls, WI (On-site)
Schedule: Monday – Friday, 8:00 AM – 4:30 PM
Position Summary
The Quality Manager is responsible for leading the Quality Management System (QMS) and ensuring all products, materials, and processes meet ISO 13485 requirements, customer specifications, regulatory standards, and internal quality expectations. This role drives continuous improvement, oversees quality assurance activities, and provides technical leadership across all quality-related functions.
Essential Duties and ResponsibilitiesQuality Management System (QMS) Leadership
- Maintain, improve, and standardize the QMS in alignment with ISO 13485 and customer regulatory requirements
- Lead continuous improvement initiatives focused on risk reduction, process capability, and operational effectiveness
- Oversee metrology, training, document control, corrective action processes, change control, and quality record retention
- Prepare for and lead internal, supplier, and customer/notified body audits
- Establish, monitor, and communicate QMS metrics, KPIs, and quality objectives
- Ensure production, inspection, and documentation activities comply with ISO 13485, customer, and regulatory requirements
- Manage nonconforming product processes including containment, disposition, root cause analysis, and CAPA
- Lead risk management activities using FMEA, control plans, and validation methodologies
- Support equipment qualification, process validation, and ongoing process monitoring
- Develop and implement quality improvement initiatives to reduce waste, improve product quality, and improve product consistency
- Partner with engineering and operations to enhance converting, slitting, printing, and laminating processes
- Drive reduction of scrap, variability, customer complaints, and internal defects
- Utilize data analysis and statistical methods to identify and implement improvements
- Evaluate, approve, and monitor suppliers of materials and outsourced services
- Conduct supplier audits and lead supplier performance improvement efforts
- Establish quality expectations and ensure incoming materials meet specifications
- Serve as the primary quality contact for customers, supporting audits, regulatory inquiries, and complaint investigations
- Lead preparation and submission of PPAP, FAI, and qualification documentation
- Communicate quality performance, improvements, and issue resolution effectively
- Supervise, train, and develop quality personnel
- Promote a culture of accountability, continuous improvement, and quality ownership
- Ensure consistent application of quality policies and procedures across the organization
Required Qualifications
- Bachelor’s degree preferred; equivalent experience considered
- 5+ years of quality experience in a regulated manufacturing environment
- Strong working knowledge of ISO 13485 within a supplier or manufacturing environment
- Experience with risk-based quality tools (FMEA, control plans, validation, SPC)
- Proven ability to lead audits and drive QMS improvements
- Strong analytical, problem-solving, and decision-making skills
- Effective communication skills with customer and auditor interaction experience
- Proficiency in Microsoft Office; experience with ERP/QMS systems preferred
Preferred Qualifications
- Experience in adhesive converting, printing, or flexible materials manufacturing
- Knowledge of medical device regulations, including 21 CFR Part 820
- Experience with PPAP, process validation, and capability analysis
- Background in supplier quality management and external auditing
Key Competencies
- Leadership and team development
- Continuous improvement mindset
- Attention to detail and documentation accuracy
- Strong organizational and project management skills
- Ability to operate in a fast-paced, customer-driven environment
- Professional and effective communication skills
Physical Requirements amp; Work Environment
- Ability to sit, stand, and walk for extended periods
- Ability to lift up to 25 pounds occasionally
- Exposure to manufacturing environments, including converting and printing equipment
- Use of required personal protective equipment (PPE)