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Quality Systems Manager Jobs in Wisconsin (NOW HIRING)

MPE-Inc

Quality Engineer

Milwaukee, WI · On-site

$74K - $95K/yr

Under the supervision of the Regulatory and Quality Systems Manager, the Quality Engineer is a development-oriented role intended to build capability across both new product development/design ...

Talnt

Quality Manager

Stevens Point, WI

$120K - $125K/yr

Build and maintain systems for nonconforming material control, Material Review Board (MRB) activities, corrective actions, and configuration management. * Develop supplier quality requirements ...

Amcor plc

Quality Manager

Madison, WI · On-site

Manage Amcor Plant Quality System and maintain registration to chosen quality standards. * Provide leadership and direction during supplier, internal and customer related quality activities, serving ...

Amcor

Quality Manager

Madison, WI · On-site

Manage Amcor Plant Quality System and maintain registration to chosen quality standards. * Provide leadership and direction during supplier, internal and customer related quality activities, serving ...

Good Culture

Quality Data Analyst

La Crosse, WI · On-site +1

Quality Systems Manager DEPARTMENT: Quality TRAVEL REQUIREMENT: 5-15% JOB PURPOSE SUMMARY: Good Culture is on a mission to zero defects - and we need a curious, data-driven thinker to help get us ...

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All JobsQuality Systems JobsQuality Systems Manager JobsQuality Systems Manager Jobs in Wisconsin

Quality Systems Manager information

See Wisconsin salary details

$54.5K

$99.5K

$155.4K

How much do quality systems manager jobs pay per year?

As of Aug 9, 2026, the average yearly pay for quality systems manager in Wisconsin is $99,536.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,200.00 and $123,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality systems manager?

To thrive as a Quality Systems Manager, you need strong expertise in quality management principles, regulatory compliance, and process improvement, typically supported by a degree in engineering or a related field. Familiarity with ISO standards (like ISO 9001), quality management software, and certifications such as Six Sigma or ASQ Certified Manager of Quality/Organizational Excellence are commonly required. Leadership, analytical thinking, and effective communication are crucial soft skills for coordinating teams and driving continuous improvement. These skills and qualifications are essential to ensure consistent product quality, regulatory adherence, and overall organizational efficiency.

What is the difference between Quality Systems Manager vs Quality Assurance Manager?

AspectQuality Systems ManagerQuality Assurance Manager
Primary FocusDeveloping and maintaining quality management systems and processesOverseeing product testing and ensuring quality standards are met during production
CertificationsISO 9001 Lead Auditor, CQEASQ certifications, QA certifications
Work EnvironmentQuality management departments, compliance teamsProduction lines, testing labs
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

While both roles focus on quality, the Quality Systems Manager primarily manages the overall quality management system and compliance, whereas the Quality Assurance Manager concentrates on product testing and ensuring quality during production. Understanding these differences helps in selecting the right career path or hiring the appropriate professional.

What does a quality systems manager do?

As a quality systems manager, your primary responsibilities are monitoring the production processes and ensuring factory machinery/goods are within company and industry requirements. Your duties include weighing, sampling, or testing products for quality and functionality. You may also report the results of quality control tests. You monitor the equipment and people involved, and help with the development and implementation of improved management systems. You are also in charge of creating a standard operating procedure for the specific plant where you work. You check that everything is running at full efficiency and the quality of merchandise is standardized.

How does a quality systems manager typically collaborate with cross-functional teams to drive continuous improvement?

A Quality Systems Manager works closely with departments such as manufacturing, engineering, regulatory, and supply chain to ensure that quality standards are consistently met and improved. They often lead or participate in cross-functional meetings to identify process gaps, analyze data, and develop corrective and preventive action plans. Effective communication and project management skills are essential, as the role involves aligning diverse teams toward common quality objectives and facilitating training or audits to support compliance and improvement initiatives.
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What cities in Wisconsin are hiring for Quality Systems Manager jobs? Cities in Wisconsin with the most Quality Systems Manager job openings:
Quality Systems Manager jobs near you
Infographic showing various Quality Systems Manager job openings in Wisconsin as of August 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 94% In-person, 3% Hybrid, and 3% Remote job distribution, with an average salary of $99,536 per year, or $47.9 per hour.

Quality Engineer

MPE-Inc

Milwaukee, WI • On-site

$74K - $95K/yr

Full-time

Re-posted 15 days ago

Job description

Job Summary:

Under the supervision of the Regulatory and Quality Systems Manager, the Quality Engineer is a development-oriented role intended to build capability across both new product development/design transfer and site quality/sustaining production. The position will partner with Engineering, Operations, Supplier Quality, Quality Systems, and other cross-functional groups to support compliant product launch, production readiness, and ongoing manufacturing quality. Primary assignments may emphasize the NPD/design transfer path or the site quality path based on business needs, individual skill set, and capacity requirements.

Essential duties and responsibilities:

  • Ensure assigned quality engineering activities comply with ISO 13485, applicable FDA/QMS requirements, customer requirements, and MPE quality system procedures.
  • Review drawings, specifications, BOMs, work instructions, test/inspection criteria, labeling, packaging, and other quality records for manufacturability, control, and objective evidence needs.
  • Support transfer and production readiness activities, including FMEA, CTQs, control plans, inspection strategy, PPAP, qualification/validation planning, and production readiness reviews.
  • Apply statistical tools to sampling plans, measurement systems (GR&R), process capability, test planning, and data review as appropriate.
  • Develop and maintain acceptance criteria, inspection/test methods, and production release evidence requirements for receiving, in-process, final inspection, and finished product release.
  • Plan, execute, and document IQ/OQ/PQ, process validation, TMV, or other qualifications as assigned.
  • Provide site quality support for production, including DHR/product release review, containment, rework/reinspection planning, NCR/MRB disposition support, and quality-related line issue resolution.
  • Lead or support investigations for nonconformances, complaints/RMAs, deviations, audit findings, and CAPAs with emphasis on containment, root cause, corrective action, and effectiveness verification.
  • Analyze manufacturing, inspection, complaint, NCR, CAPA, and qualification data to identify trends and support risk-based quality improvements.
  • Support handoff between NPD, sustaining production, and site quality teams, including early-life production monitoring after launch.
  • Perform other duties to support the QMS as assigned.

An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.

The above list reflects the general details necessary to describe the principle and essential functions of the position and shall not be construed as the only duties that may be assigned for the position.

Minimum/Preferred Qualifications:

Education

  • Bachelor’s degree in Engineering, Quality, Science, or related technical discipline, or equivalent combination of education and experience.

Experience and/or Training

  • 0-3 years of experience in manufacturing engineering or quality assurance.
  • Working knowledge of quality engineering methods such as risk management, FMEA, control plans, NCR/CAPA, root cause analysis, sampling plans, GR&R, capability, PPAP/FAI, and qualification/validation.
  • Familiar with FDA regulations and ISO 13485.
  • Ability to prepare clear technical justifications, investigation summaries, qualification/test reports, and quality records suitable for audit or customer review.
  • Familiar with change control, document control, ERP/MRP systems, inspection planning, and production floor support.
  • Preferred candidates hold a Certified Quality Engineer (CQE), Lean/Six Sigma, or similar quality certification.

Physical and mental demands

  • Continuous- Sitting, seeing, hearing, speaking, reading, computer use, comprehension
  • Frequent- Critical thinking, problem solving, reasoning, complex information processing
  • Occasional- Decision making
  • Intermittent- fine motor skills for manipulating tools or equipment, lifting up to 30 lbs., walk and stand for inspections

The mental and physical requirements described here are representative of those that must be met by an individual to successfully perform the essential functions of this position.