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Qms Manager Jobs in Racine, WI (NOW HIRING)

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 ...

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 ...

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

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 ...

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Qms Manager information

See Racine, WI salary details

$22.5K

$80.8K

$148.2K

How much do qms manager jobs pay per year?

As of Jun 14, 2026, the average yearly pay for qms manager in Racine, WI is $80,790.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,300.00 and $127,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a QMS Manager, and why are they important?

To thrive as a QMS Manager, you need expertise in quality management systems, regulatory compliance, and process improvement, typically supported by a relevant degree and experience in quality assurance. Familiarity with ISO standards (such as ISO 9001), audit management tools, and quality software platforms is essential. Strong leadership, problem-solving skills, and effective communication help drive a culture of continuous improvement and team alignment. These competencies ensure that organizational processes meet regulatory requirements and consistently deliver high-quality outcomes.

How does a QMS Manager typically collaborate with other departments to ensure compliance and continuous improvement?

A QMS Manager regularly works cross-functionally with departments such as production, engineering, and procurement to implement and maintain quality standards. This involves coordinating audits, facilitating training sessions, and gathering feedback to identify areas for process improvement. Effective communication and negotiation skills are essential, as the QMS Manager must align diverse teams toward compliance goals and foster a culture of continuous improvement. Regular meetings and collaborative problem-solving are part of ensuring that quality objectives are met across the organization.

What are QMS Managers?

QMS Managers, or Quality Management System Managers, are professionals responsible for developing, implementing, and overseeing an organization's quality management system. They ensure that processes and products meet established quality standards and comply with relevant regulations. Their duties often include conducting audits, managing documentation, training staff on quality procedures, and driving continuous improvement initiatives. QMS Managers play a crucial role in maintaining customer satisfaction and supporting organizational efficiency.

What is the difference between Qms Manager vs Quality Assurance Supervisor?

AspectQms ManagerQuality Assurance Supervisor
CertificationsISO 9001 Lead Auditor, CQEISO 9001 Lead Auditor, CQE
Work EnvironmentOversees quality management systems across departmentsSupervises quality assurance team and daily testing activities
Industry UsageUsed in manufacturing, aerospace, automotiveCommon in manufacturing, pharmaceuticals, food industry
Primary FocusDeveloping, maintaining, and improving QMSMonitoring 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.

What are popular job titles related to Qms Manager jobs in Racine, WI? For Qms Manager jobs in Racine, WI, the most frequently searched job titles are:
What job categories do people searching Qms Manager jobs in Racine, WI look for? The top searched job categories for Qms Manager jobs in Racine, WI are:
What cities near Racine, WI are hiring for Qms Manager jobs? Cities near Racine, WI with the most Qms Manager job openings:
Infographic showing various Qms Manager job openings in Racine, WI as of June 2026, with employment types broken down into 100% Full Time. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $80,790 per year, or $38.8 per hour.

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
Quality Assurance amp; Regulatory Compliance
  • 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
Continuous Improvement amp; Process Effectiveness
  • 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
Supplier Quality Management
  • 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
Customer Interaction amp; Technical Support
  • 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
Leadership amp; Team Development
  • 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)