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Quality Systems Manager Jobs in Butler, WI (NOW HIRING)

MPE-Inc

Quality Systems Specialist

Milwaukee, WI · On-site

$75K - $85K/yr

Why This Role Every great medical device company runs on a strong Quality Management System behind the scenes -- and that's where you come in. As our Quality Systems Specialist, you'll help keep MPE ...

Grover Corporation

Quality Engineer

Glendale, WI · On-site

$70K - $91K/yr

Quality Engineer Grover Corporation -- Glendale, WI Reports to ... Operations Systems Manager Team: Individual Contributor (No Direct Reports) Summary Grover ...

ATI

Quality Management Systems Specialist

Cudahy, WI · On-site

The Quality Systems Specialist position reports to the Manager, Quality. As a successful Quality systems Specialist, you will manage the activities associated with the development, maintenance ...

ATI

Quality Management Systems Specialist

Cudahy, WI · On-site

The Quality Systems Specialist position reports to the Manager, Quality. As a successful Quality systems Specialist, you will manage the activities associated with the development, maintenance ...

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 ...

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All JobsQuality Systems JobsQuality Systems Manager JobsQuality Systems Manager Jobs in Butler, WI

Quality Systems Manager information

See Butler, WI salary details

$53K

$96.9K

$151.2K

How much do quality systems manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for quality systems manager in Butler, WI is $96,851.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,200.00 and $120,300.00 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.
More about Quality Systems Manager jobs
What cities near Butler, WI are hiring for Quality Systems Manager jobs? Cities near Butler, WI with the most Quality Systems Manager job openings:
Quality Systems Manager jobs near you
Infographic showing various Quality Systems Manager job openings in Butler, WI as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $96,851 per year, or $46.6 per hour.

Quality Systems and Compliance Manager

MGS Mfg. Group, Inc

Germantown, WI

Full-time

Re-posted 15 days ago

Job description

MGS has an exciting opportunity for an experienced Quality Systems and Compliance Manager to join our MGS Germantown team. 

The Quality Systems and Compliance Manager is responsible for maintaining and developing the corporate quality system as it pertains to the streamlining and standardization of specific quality activities at each of MGS' Manufacturing locations. Key responsibilities are to support the Director of Quality Systems & Compliance in their efforts to further progress projects across multiple manufacturing sites and regions that increase MGS efficiency, regulatory compliance, quality control and overall alignment to one standard process.

  • Execute Quality department projects to completion with minimal supervision
  • Communicate with and influence multiple functional leaders
  • Manage the document control software and apply best practices
  • Execute Internal Audits in compliance with ISO14001, ISO9001, or 13485 (as applicable) and corporate policies.
  • Assist with external audits from Regulatory bodies or customers
  • Collaborate on corrective action plans related to audit findings
  • Understand workflows and approval cycles for controlled documents
  • Compose procedures, SOP, Work Instruction or Policies that have a multi-site impact
  • Review and approval of corporate quality system documents
  • Manage the project rollout of new e-QMS modules across multiple sites
  • Support with the onboarding or ramp of new sites in relation to preparing the site for inspection and commercial activities, including QMS and records review.
  • Manage all records related to the Corporate Quality system.
  • Report on project updates and QMS software analytics
  • Analyze manufacturing quality processes such as batch release, CAPA, Hold Material and validation in order to recommend improvement
  • Any other duties as assigned.

ABOUT MGS:

As a global provider of healthcare manufacturing solutions, MGS provides the right balance to drive vital innovations: robust end-to-end solutions combined with the strong customer focus and seamless collaboration of an agile partner. That's why we're the engineering and manufacturing partner of choice for today's leading Pharma, Diagnostic and MedTech innovators. Serving customers from 12 strategically located facilities around the world, we transform our customers' most pressing challenges into innovations that improve lives.   To learn more about MGS, please visit  www.mgsmfg.com.


A qualified Quality Systems and Compliance Manager would fulfill these requirements:

  • Completion of a bachelor's degree in Pharmaceutical, Medical Device, or engineering discipline.
  • Experience with Quality System Management, ideally ISO13485
  • At least 5 years' experience working within a Quality systems, project or day to day quality role within a regulated manufacturing environment
  • Proficient in Microsoft Office Applications
  • Professional verbal and written communication
  • Excellent attention to detail and accuracy
  • Ability to multi-task and prioritize
  • Ability to read, write, comprehend, and communicate the Spanish language in a proficient manner is preferred.

MGS is an Equal Opportunity Employer.