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Quality Systems Manager Jobs in Minnesota (NOW HIRING)

Protolabs

Quality Systems Engineer

Rosemount, MN · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

What You Will Do Quality Management System (Core Responsibility) * Manage, maintain, and improve the company's QMS in alignment with ISO 9001, ISO 13485, AS9100, and internal procedures * Identify ...

Protolabs

Quality Systems Engineer

Plymouth, MN · On-site +1

$69K - $92K/yr

What You Will Do Quality Management System (Core Responsibility) * Manage, maintain, and improve the company's QMS in alignment with ISO 9001, ISO 13485, AS9100, and internal procedures * Identify ...

Protolabs

Quality Systems Engineer

Plymouth, MN · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

What You Will Do Quality Management System (Core Responsibility) * Manage, maintain, and improve the company's QMS in alignment with ISO 9001, ISO 13485, AS9100, and internal procedures * Identify ...

Protolabs

Quality Systems Engineer

Maple Plain, MN · On-site +1

$69K - $92K/yr

What You Will Do Quality Management System (Core Responsibility) * Manage, maintain, and improve the company's QMS in alignment with ISO 9001, ISO 13485, AS9100, and internal procedures * Identify ...

Abbott

Quality Systems Specialist

Saint Paul, MN · On-site

$61K - $122K/yr

  • Medical

  • Retirement

Document quality issues and performance measures for management review. * May liaise with external ... Quality Systems experience within Medical Devices, a plus. * Experience with one or more of the ...

Actalent

Quality Systems Specialist

Lakeville, MN · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Administer and maintain Quality Management System (QMS) programs, systems, and tools to support ongoing quality and food safety initiatives. * Own system and database administration activities ...

New

Abbott

Quality Systems Specialist

Saint Paul, MN · On-site

$61K - $122K/yr

  • Medical

  • Retirement

Document quality issues and performance measures for management review. * May liaise with external ... Quality Systems experience within Medical Devices, a plus. * Experience with one or more of the ...

Abbott

Quality Systems Specialist

Saint Paul, MN · On-site

$61K - $122K/yr

  • Medical

  • Retirement

Document quality issues and performance measures for management review. * May liaise with external ... Quality Systems experience within Medical Devices, a plus. * Experience with one or more of the ...

Conagra Brands, Inc.

Quality Systems Specialist

North Mankato, MN · On-site

$28/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Shift: 6:00 AM-2:30 PM Hourly Rate: $28.00 an hour Reporting to the Plant Quality Manager, you will ... Serve as document controller for food safety and quality systems, including maintaining, writing ...

Conagra Brands

Quality Systems Specialist

North Mankato, MN · On-site

$28/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Shift: 6:00 AM-2:30 PM Hourly Rate: $28.00 an hour Reporting to the Plant Quality Manager, you will ... Serve as document controller for food safety and quality systems, including maintaining, writing ...

Protolabs

Quality Program Manager

Plymouth, MN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 cross ...

Protolabs

Quality Program Manager

Plymouth, MN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 cross ...

Protolabs

Quality Program Manager

Plymouth, MN

$76K - $102K/yr

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 cross ...

Elemet Group

Quality Systems & Compliance Manager

Aitkin, MN · On-site

$75K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Own the Quality System that Powers Precision Manufacturing Step into Elemet Manufacturing as the leader who stewards our Quality Management System (QMS) and elevates product and process compliance ...

New

Baxter

Sr. Analyst, Quality Systems

Saint Paul, MN

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

This role owns and advances key Quality Systems, including Training, Document Control, Change ... Manage and enhance the training program, ensuring system effectiveness, compliance with ...

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Showing results 21-40

All JobsQuality Systems JobsQuality Systems Manager JobsQuality Systems Manager Jobs in Minnesota

Quality Systems Manager information

See Minnesota salary details

$52.9K

$96.6K

$150.8K

How much do quality systems manager jobs pay per year?

As of Aug 12, 2026, the average yearly pay for quality systems manager in Minnesota is $96,583.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,900.00 and $120,000.00 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 are the most commonly searched types of Quality Systems jobs in Minnesota? The most popular types of Quality Systems jobs in Minnesota are:
What are popular job titles related to Quality Systems Manager jobs in Minnesota? For Quality Systems Manager jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Quality Systems Manager jobs in Minnesota look for? The top searched job categories for Quality Systems Manager jobs in Minnesota are:
What cities in Minnesota are hiring for Quality Systems Manager jobs? Cities in Minnesota with the most Quality Systems Manager job openings:
Quality Systems Manager jobs near you
Infographic showing various Quality Systems Manager job openings in Minnesota as of August 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 99% In-person, and 1% Hybrid job distribution, with an average salary of $96,583 per year, or $46.4 per hour.

Quality Systems Specialist II

Imricor Medical Systems Inc

Burnsville, MN • On-site

$75K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 22 days ago

Job description

Job Type
Full-time
Description
Supervisor's Title: Quality Director
Exempt or Non-Exempt: Exempt
Location: Must be able to work at our Burnsville location.
Compensation: The expected salary/wage for this Minnesota-based position is between $75,000-110,000. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's knowledge, skills, and or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, and Retirement Benefits).
Basic Function
The Quality Systems Specialist II position is responsible for the support of a compliant and effective quality management system. Primary quality system functions include Corrective Action and Preventive Action (CAPA), Nonconformance Management, Internal and External Audit, Document and Records Management, Change Control, Training, and Quality Metric Analysis and Review.
Responsibilities
  • Develops and maintains quality system procedures to ensure compliance with regulations and industry standards.
  • Participates in internal and external quality audits to ensure compliance with regulations and standards.
  • Participates in, or leads, the completion of CAPA projects, assuring compliance, quality, and timeliness of records.
  • Investigate and resolve quality issues, including conducting root cause analysis and implementing corrective and preventive actions.
  • Leads meetings and communications for CAPA updates, information, and concerns.
  • Monitors and analyzes quality metrics to identify areas for improvement and initiate corrective actions.
  • Provides backup support for engineering change orders and other document change requests.
  • Develops and maintains electronic quality management system processes. Provides cross-functional training and support as needed.
  • Collaborates with cross-functional teams to ensure quality standards are met throughout the product lifecycle.
  • Communicates quality system updates and changes to relevant stakeholders.
  • Provides guidance and training to the organization on quality system requirements and best practices.
  • Performs other duties as assigned.

Requirements
Qualifications
• Bachelor's degree in a related technical field.
  • 3-5 years of experience in quality assurance or other quality systems roles in the medical device industry.
  • Previous CAPA and nonconformance experience and demonstrated use of quality tools and methodologies.
  • Detailed knowledge of 21 CFR Part 820, ISO 13485, EU MDR, and other global regulatory requirements.
  • Advanced computer skills, including statistical/data analysis and report writing skills.
  • Strong verbal and written communication skills.
  • Excellent attention to detail. Multitasks prioritize and meet deadlines promptly.

Working Conditions
• Light work, exerting up to 20 lbs. of force or less.
• 85% of time requires viewing and working at computer screen.
The statements above reflect the principal function and most significant duties of the job as necessary for its evaluation in relation to other jobs in the organization and shall not be construed as a detailed description of all the work requirements that may be inherent in the job. Any functions that are non-Essential will be identified as such above. A request for Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
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About Imricor

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

51 - 200 Employees

Headquarters location

Burnsville, MN, US

Year founded

2006

Social media

Twitter

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