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Quality Management System Manager Jobs in Minnesota

Quality Systems Manager

Maple Grove, MN · On-site

$120K - $140K/yr

The role is also responsible for the selection, implementation, administration, and monitoring of the Quality Management System ensuring continual compliance of the organization. The role owns the ...

Quality Systems Manager

Osseo, MN · On-site

$120K - $140K/yr

The role is also responsible for the selection, implementation, administration, and monitoring of the Quality Management System ensuring continual compliance of the organization. The role owns the ...

Quality Systems Manager

Maple Grove, MN · On-site

$120K - $140K/yr

The role is also responsible for the selection, implementation, administration, and monitoring of the Quality Management System ensuring continual compliance of the organization. The role owns the ...

Quality Manager

Aitkin, MN

$36.06 - $43.27/hr

Monitor, improve, and maintain policies and procedures, with a continual focus on developing and evolving the Quality Management System (QMS). Ensure that the QMS is effectively executed and ...

Champion best practices in quality systems management, helping Protolabs scale its quality ... capabilities while maintaining a culture of excellence and innovation. What You Will Do: * Support ...

Support the administration and maintenance of a harmonized Quality Management System (QMS) across multiple manufacturing sites. * Coordinate quality system processes including document control ...

Champion best practices in quality systems management, helping Protolabs scale its quality ... capabilities while maintaining a culture of excellence and innovation. What You Will Do: * Support ...

Champion best practices in quality systems management, helping Protolabs scale its quality ... capabilities while maintaining a culture of excellence and innovation. What You Will Do: * Support ...

This role maintains and enhances the Quality Management System (QMS) in alignment with FDA 21 CFR Part 820 and other applicable medical technology regulations, while driving continuous improvement ...

... Management System (QMS) within the business unit to ensure consistent production of products and processes that meet established standards and customer requirements. The role includes the overall ...

Quality Manager

Owatonna, MN · On-site

$95K - $115K/yr

Provide hands-on management of the elements of the Quality Management System (QMS), to include quality action plans, corrective actions, supplier quality management, customer complaints, standard ...

Quality System Oversight * Maintain and lead an audit-ready AS9100/ISO9001 Quality Management System * Oversee compliance with REACH, RoHS, sustainability, and environmental reporting * Manage ...

Quality Control Manager

Saint Paul, MN · On-site

$120K - $140K/yr

Knowledge of QMS, audits, quality systems, and regulatory compliance. * Bachelor's degree in Quality Management, Engineering, Business, or a related field preferred. This is a direct hire, long term ...

Quality Manager

Owatonna, MN · On-site

$95K - $115K/yr

Provide hands-on management of the elements of the Quality Management System (QMS), to include quality action plans, corrective actions, supplier quality management, customer complaints, standard ...

Quality Manager

Owatonna, MN · On-site

$95K - $115K/yr

Provide hands-on management of the elements of the Quality Management System (QMS), to include quality action plans, corrective actions, supplier quality management, customer complaints, standard ...

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Quality Management System Manager information

What is the difference between Quality Management System Manager vs Quality Assurance Manager?

AspectQuality Management System ManagerQuality Assurance Manager
Primary FocusDeveloping, implementing, and maintaining quality management systemsOverseeing quality assurance processes and testing
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentQuality departments, compliance teamsProduction, manufacturing, or service delivery areas
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

The Quality Management System Manager focuses on establishing and maintaining comprehensive quality systems, ensuring compliance with standards like ISO 9001. In contrast, the Quality Assurance Manager concentrates on testing, inspections, and ensuring products or services meet quality requirements. Both roles are essential for quality improvement but differ in scope and daily responsibilities.

What are the most commonly searched types of Quality Management System jobs in Minnesota? The most popular types of Quality Management System jobs in Minnesota are:
What cities in Minnesota are hiring for Quality Management System Manager jobs? Cities in Minnesota with the most Quality Management System Manager job openings:
Infographic showing various Quality Management System Manager job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 days ago


Job description

Overview

About Cretex Medical: 

Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry.  Our customers view us as a trusted partner in the areas of injection molding, laser processing, metal stamping and device assembly.  Learn more at www.cretexmedical.com.

Quality Systems Manager Position Summary:

The Quality Systems Manager is responsible for the development, implementation, maintenance, and continuous improvement of the Quality Management System (QMS) in compliance with applicable regulatory requirements (e.g., FDA 21 CFR Part 820, ISO 13485, and other global standards). Key responsibilities include managing Document Control and CAPA functions, ensuring robust governance, timely execution, and effectiveness of quality system processes. The role partners cross-functionally with Operations, Engineering, and Supply Chain to embed quality into all stages of the product lifecycle and to support audit readiness and inspection success. 

Responsibilities
  • Audit Leadership & Regulatory Readiness Provide leadership oversight to second- and third-party audits, including preparation, execution, reporting, and closure of audit findings. Ensure sustained inspection of readiness and successful outcomes with regulatory bodies and customers.  
  • Internal Audit Program Management Provide leadership oversight the internal audit program, including auditor selection, training, audit scheduling, execution, and driving timely and effective corrective actions to strengthen the QMS.  
  • QMS Compliance & Continuous Improvement Develop, maintain, and continuously improve a robust Quality Management System compliant with ISO 13485, FDA 21 CFR Part 820, and applicable global regulations, ensuring scalability with organizational growth.  
  • CAPA & Complaint Management Oversight Lead CAPA facilitators and ensure effective management of customer complaints and internal CAPAs, including root cause analysis, corrective/preventive actions, effectiveness checks, and trend analysis.  
  • Process & Product Quality Improvement Conduct process and product audits to identify gaps and drive continuous improvement initiatives using Lean and risk-based methodologies.  
  • Regulatory & Customer Interface Provide leadership in regulatory matters and serve as a key quality representative to customers, ensuring alignment with regulatory requirements and customer expectations.  
  • Global QMS Strategy & Standardization Establish and maintain a global QMS framework that supports multi-site operations, harmonization, and future growth, including acquisitions and integration efforts.  
  • Supplier Quality Integration Represent Quality on the Supplier Qualification Team & supplier performance reviews, ensure that Approved Supplier List (ASL), and supplier audits meets regulatory standards. 
  • Training & Quality Culture Development Develop and sustain QMS training programs to drive compliance, enhance quality awareness, and build a culture of accountability and continuous improvement.  
  • Cross-Functional Collaboration Partner with Quality, Operations, Engineering, and other functions to implement QMS improvements that enhance efficiency, compliance, and product quality.  
  • Digital QMS Systems Management Implement, maintain, and optimize Global QMS software, ensuring system effectiveness, data integrity, and user adoption.  
  • Management Review & Metrics Support preparation and presentation of Management Review inputs, ensuring clear visibility to QMS performance, risks, and improvement opportunities.  
  • Team Leadership & Development Lead, coach, and mentor the QMS team, fostering a high-performing organization with strong accountability, engagement, and capability development. 
Qualifications

Quality Systems Manager Requirements: 

  • Bachelor's degree or 6 years of equivalent work experience
  • 5 years of experience managing quality management systems
  • Experience with ISO 13485:2016 and FDA
  • Lead Auditor Certification
  • Ability to consistently achieve short and long-term business results
  • Ability to prioritize work and manage multiple tasks when needed
  • Ability to follow through on commitments and hold team members accountable
  • Consistently produces work that meets the customer's requirements
  • Project management skills
  • Microsoft Office proficiency (Outlook, Word, Excel, PowerPoint, Publisher)
  • Clear and effective verbal and written communication skills
  • Attention to detail
  • Organizational skills
  • Ability to work in a fast-paced team environment
  • Ability to prioritize and multitask

Quality Systems Manager Preferred Requirements: 

  • Quality systems experience in a manufacturing setting
  • Continuing education; including participation in local chapters, associations, and/or organizations

What is it like to work at Cretex Medical?

We recognize the contribution of every individual and promote growth, safety and security for all our employees. Cretex Medical values performance and pays competitive wages along with a rich benefit package. We offer a positive work environment with a focus on continuous improvement.

Here are some of things that employees have said about working for Cretex Medical:

  • "The culture at Cretex is collaborative. Everyone here is willing to help you whether it is a director, a machinist, or your boss. Everyone is always willing to help you figure out a project and get it done right."
  • "I would tell potential interns that Cretex is a great company to work for. It has set a high bar for corporate culture as well as the quality of work you can do. I would definitely recommend it."
  • "I learned that I really like the medical device industry. The importance and the gravity of what we do here is felt by the employees. You can have that passion in your work because you know what you are striving for is to save lives."

We encourage you to explore the many opportunities Cretex Medical can offer you as a valued team member.

#LI-JW1

Pay RangeUSD $100,900.00 - USD $151,300.00 /Yr.Pay Range Details

This pay range reflects the base hourly rate or annual salary for positions within this job grade, based on our market-based pay structures. Actual compensation will depend on factors such as skills, relevant experience, education, internal equity, business needs, and local market conditions. While the full hiring range is shared for transparency, offers are rarely made at the minimum or maximum of the range.

Company Benefits

Compensation:

This is a bonus eligible postion.

All Employees:

Our 401k retirement savings plan with a company match contribution; onsite health clinics, discretionary holiday bonus program (based on years of service), Cretex University, 24/7 employee assistance program with access to five confidential visits with a licensed counselor at no cost, wellness program with incentives, an employee death benefit, and employee sick and safe leave are available to all Cretex employees. 

 

20+hours:

Cretex's medical benefit package includes: comprehensive medical insurance with access to virtual providers; dental insurance (Little Partners Dental benefit covers services 100 percent for children 12 and younger when seen by a Health Partners in network provider); vision insurance; a pre-tax health savings account, healthcare and dependent care pre-tax reimbursement accounts; paid holidays, paid time off; and our discretionary profit sharing program are available to employees working 20+ hours/week. 

30+ hours:

Parental Leave, accident and critical illness benefits, optional employee, spouse, and child life; short and long term disability; company provided life insurance; and tuition assistance programs are available to employees working 30+ hours per week. 

(Some benefits are subject to eligibility criteria.)

Applicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, gender identity, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law.  

Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify. 

Employment Type: FULL_TIME