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Quality Systems Manager Jobs in Wisconsin (NOW HIRING)

amphenol

Quality Systems Engineer

Janesville, WI · On-site

This role leads internal audit activities, supports external certification audits, manages quality system documentation, and works cross-functionally to drive corrective action and continuous ...

Amphenol

Quality Systems Engineer

Janesville, WI · On-site

$74K - $85K/yr

This role leads internal audit activities, supports external certification audits, manages quality system documentation, and works cross-functionally to drive corrective action and continuous ...

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 ...

Promega

Quality Systems Project Employee

Madison, WI · On-site

... to management or other stakeholders. 8. Completes actions assigned from audits, deviations, changes, nonconformances, etc. 9. Represents Quality Systems in special projects as assigned. 10. ...

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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 13, 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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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.

Systems Manager - Quality

Rockline Industries

Sheboygan, WI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Rockline Industries rating

6.8

Company rating: 6.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

Job description

What You'll Do

As a key member of the Quality team, you will oversee core quality system processes including CAPA, change management, customer complaints, product release, internal auditing, document control, and regulatory readiness. You will play an important role in ensuring compliance with FDA regulations, customer requirements, and internal quality standards while helping drive continuous improvement across the facility.

Quality Systems Leadership
  • Develop and manage deviation, non-conformance, investigation, and CAPA processes.
  • Lead and maintain the site's Change Management program.
  • Oversee customer complaint management, including investigations, trend analysis, reporting, and corrective actions.
  • Manage product release activities, batch record review processes, quality metrics, and customer Certificates of Analysis (CoAs).
  • Coordinate Annual Product Reviews and Quarterly Management Reviews.
  • Administer the Document Control program, including change control activities and system metrics.
  • Lead the Internal Auditing program, including auditor training, audit execution, system development, and reporting.
Regulatory Compliance & Continuous Improvement
  • Partner closely with Quality Operations, Quality Laboratory, and Manufacturing teams to ensure effective and compliant quality systems.
  • Serve as a key participant during FDA inspections, customer audits, and third-party regulatory audits.
  • Manage GMP and sanitation programs and improvement initiatives.
  • Drive a culture of quality, compliance, and operational excellence throughout the organization.
Team Leadership
  • Develop, coach, and manage direct reports.
  • Foster collaboration and accountability while supporting Rockline's RRITE values of Renew, Respect, Integrity, Teamwork, and Excellence.
What We're Looking ForRequired Qualifications
  • Bachelor's degree in Chemistry, Microbiology, Biology, Engineering, or a related scientific discipline.
  • Minimum of seven years of experience supporting quality assurance systems within pharmaceutical, medical device, or other FDA-regulated manufacturing environments.
  • Minimum of three years of leadership experience or experience serving in an advisory capacity.
  • Five or more years of experience interacting with regulatory agencies or regulatory bodies, such as the FDA or TGA.
  • Demonstrated experience with:
    • Root cause analysis
    • Risk analysis methodologies
    • CAPA management
    • Regulatory investigations
    • Internal and external audits
    • Document control systems
    • Change management
    • Complaint management
    • Deviation and non-conformance programs
Preferred Qualifications
  • Advanced degree in a scientific or related discipline.
Why Join Rockline?

Rockline Industries is a privately held manufacturer and distributor of consumer packaged goods with a long-standing reputation for innovation, quality, and customer partnership. Our associates help produce products used by millions of consumers every day.

When you join Rockline, you'll find:

  • A stable, privately held organization focused on long-term success
  • Opportunities to make a meaningful impact in a highly regulated manufacturing environment
  • Cross-functional collaboration with operations, quality, laboratory, and leadership teams
  • A culture built around our RRITE values: Renew, Respect, Integrity, Teamwork, and Excellence
  • Career growth and development opportunities within a global manufacturing organization

With headquarters in Sheboygan, Wisconsin, Rockline employs more than 800 associates locally and thousands globally, supporting customers and consumers across North America and beyond.

Benefits That Support You

We offer a comprehensive benefits package designed to support your health, financial security, and work-life balance, including:

Health & Wellness:
  • Medical, dental, and vision coverage
  • Wellness programs
  • Fitness reimbursement
Financial Security
  • Retirement savings plan with company match
  • Life and disability insurance
  • Optional supplemental coverage
Career & Lifestyle
  • Paid time off starting on your first day
  • Education reimbursement
  • Employee discount programs
Mental Health Support
  • Confidential counseling and resources for personal and work-life needs

FLSA Status:  Exempt

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