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Qms Manager Jobs in Racine, WI (NOW HIRING)

Smiths Machine

Quality Engineer II

Kenosha, WI

$70K - $90K/yr

... Management System (QMS) to ensure compliance to procedural, customer, and regulatory requirements. • Fully versed in Document Control processes and procedures. • Assists in reviewing and revising ...

MPD Integration LLC

Quality Engineer 1

Cudahy, WI · On-site

$70K - $91K/yr

Maintain and support the continuous improvement of the company's Quality Management System (QMS) in accordance with ISO 9001 requirements. * Participate in internal and external quality audits and ...

ARCH Global Precision

Quality Engineer II

Kenosha, WI · On-site

$70K - $90K/yr

... Management System (QMS) to ensure compliance to procedural, customer, and regulatory requirements. • Fully versed in Document Control processes and procedures. • Assists in reviewing and revising ...

The Walsh Group

Quality Manager I

Mount Pleasant, WI · On-site

The Quality Manager I is responsible for implementation, improvement and execution of the Quality management systems (QMS) and project specific quality program requirements. They ensure that the ...

Midway Staffing

QA Specialist

Franksville, WI · On-site

... QMS systems preferred. * Internal auditing experience or certification preferred. * Ability to interpret technical and regulatory requirements and communicate effectively with employees, management ...

Agiliti

New Product Cost Engineer

Wauwatosa, WI · On-site

Agiliti is a leading provider of healthcare technology management and service solutions, helping ... Own engineering changes (ECRs/ECOs) in SolidWorks, ensuring compliance with ISO, IEC, FDA, and QMS ...

New

Gehc

Manufacturing Engineer Tube Teardown

Oak Creek, WI · On-site

$69K - $89K/yr

Project management experience. * Experience working within a Quality Management System (QMS). * Experience in a regulated manufacturing environment. * Experience working with large mechanical ...

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All JobsQms JobsQms Manager JobsQms Manager Jobs in Racine, WI

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 Sep 15, 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 is a QMS manager?

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.

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 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.

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:

Qms Manager jobs near you
Infographic showing various Qms Manager job openings in Racine, WI as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Contract, and 2% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $80,790 per year, or $38.8 per hour.

Quality Engineer II

Kenosha, WI

Smiths Machine
See more jobs at Smiths Machineexternal

$70K - $90K/yr

Full-time

Re-posted 8 days ago

Job description

Primary Responsibilities

• Self-starter, working independently on assigned projects, leading the team and collaborating with other internal and external parties.
• Plans, coordinates, and directs quality control programs designed to ensure continuous production of products consistent with established FDA and ISO standards.
• Investigates and addresses customer complaints (CAPA) regarding quality.
• Assists with internal/external audits of the Quality Management System (QMS) to ensure compliance to procedural, customer, and regulatory requirements.
• Fully versed in Document Control processes and procedures.
• Assists in reviewing and revising processes within the QMS (Quality Management System).
• Provides inspection activity for products throughout the production cycle.
• Creates, implements, updates and maintains work instructions, partnering with the Engineering and other departments.
• Creates and directs process/equipment validations (IQ, OQ, PQ).
• Reviews customer contracts (purchase orders, regulatory requirements, blueprints).
• Creates PPAP documentation (GR&R, control plans, first article inspection, criteria, etc.).
• Directs workers engaged in inspection and testing activities to ensure continuous control over materials, facilities, and products.
• Trains quality and other departments to achieve quality standards (visual and dimensional).
• Works with suppliers to ensure quality of all purchased parts for company use.
• Helps reduce scrap/waste, cost, time; drives for continuous improvement.
• Reliable, timely, ethical and consistent attendance.
• Travels to another facility and/or customer/vendor sites based on company needs.
• Other duties as assigned.

Qualifications

  • Bachelor’s degree in Quality Engineering, Mechanical Engineering, Biomedical Engineering, or a related field preferred or equivalent experience
  • five to seven years of experience in medical device manufacturing industry and in the quality engineering role, and/or training,
  • or equivalent combination of education and experience.
  • Knowledge of the medical device manufacturing industry is highly preferred.
  •  Experience with CNC machining and mechanical inspection is preferred.
  • Knowledge of ISO 13485 Quality Management System & FDA 21CFR 820 Regulations.
  • Knowledge of Geometric Dimensioning and Tolerancing per ASME Y14.5M.
  • Familiarity with test methods and standards for the design, verification, and validation of medical device products.

Language Ability
Ability to read, analyze, and interpret common scientific and technical manuals, training materials, financial reports, and legal documents (specifically in English). Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community (specifically in English). Ability to communicate effectively with tact, respect and professionalism within all levels of the organization. Must work responsibly with or without supervision using effective communication skills; able to collaborate with various departments and all levels of team members.

Computer Skills
To perform this job successfully, an individual should have professional and working knowledge of Microsoft office and its applications (Word, Excel, Power Point, etc.), e-mail, communication platforms (Zoom, Teams). Knowledge of manufacturing software and ERP systems (EPICOR is strongly preferred).

Certificates and Licenses
No certifications required. Relevant certifications demonstrating applied understanding of medical device quality system requirements, such as AAMI Quality System, Certified ASQ or ISO Lead Auditor and Regulatory Affairs Professional Society (RAPS) preferred. GD&T certifications are highly preferred.

Managing Responsibilities
No direct reports.

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