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Quality System Manager Jobs in Colorado (NOW HIRING)

Senior Director, Quality

Westminster, CO · On-site

$197K - $285K/yr

Develops, implements, and oversees a Quality Management System that complies with domestic and international regulations and standards for drug and/or medical devices. * Oversees customer product ...

This role will own the full quality system for Oribi and is critical to developing a robust quality management system that meets OEM expectations, supports IATF 16949 certification compliance, and ...

Quality Manager

Commerce City, CO · On-site

$100K - $150K/yr

This role will own the full quality system for Oribi and is critical to developing a robust quality management system that meets OEM expectations, supports IATF 16949 certification compliance, and ...

Design Quality Engineer III

Boulder, CO

$74K - $96K/yr

Qualifications Working knowledge of the FDA Quality System Regulation, ISO 13485, and the Medical Device Directive Skilled in product risk assessment (ISO 14971), requirements management and tracing ...

Desgin Quality Engineer

Boulder, CO

$74K - $96K/yr

Working knowledge of the FDA Quality System Regulation, ISO 13485, and the Medical Device Directive Skilled in product risk assessment (ISO 14971), requirements management and tracing, defect ...

This position is an integral part in sustaining and improving our quality system for expansion ... Manage and maintain all Quality Control documentation and all Quality Control activities.

This position is an integral part in sustaining and improving our quality system for expansion ... Manage and maintain all Quality Control documentation and all Quality Control activities.

Quality Engineer

Englewood, CO · On-site

$71K - $91K/yr

Provide education and guidance as needed to management and staff for Quality Systems processes, quality assurance activities, and compliance with applicable regulations and standards * Conduct new ...

Quality Engineer

Englewood, CO · On-site

$70K - $88K/yr

Provide education and guidance as needed to management and staff for Quality Systems processes, quality assurance activities, and compliance with applicable regulations and standards * Conduct new ...

Provide education and guidance as needed to management and staff for Quality Systems processes, quality assurance activities, and compliance with applicable regulations and standards * Conduct new ...

Provide education and guidance as needed to management and staff for Quality Systems processes, quality assurance activities, and compliance with applicable regulations and standards * Conduct new ...

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Showing results 1-20

Quality System Manager information

See Colorado salary details

$56.8K

$103.7K

$161.9K

How much do quality system manager jobs pay per year?

As of Jul 17, 2026, the average yearly pay for quality system manager in Colorado is $103,693.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,400.00 and $128,800.00 per year, depending on experience, location, and employer.

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

AspectQuality System ManagerQuality Assurance Manager
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentOversees quality management systems across departmentsFocuses on product quality and testing processes
Industry UsageCommon in manufacturing, aerospace, automotivePrevalent in manufacturing, healthcare, software
Primary FocusMaintaining and improving quality management systemsEnsuring product quality through testing and inspection

The Quality System Manager primarily manages the overall quality management system, ensuring compliance with standards like ISO 9001. The Quality Assurance Manager concentrates on product quality, testing, and inspection processes. Both roles require similar certifications and are vital in manufacturing and related industries, but their focus areas differ—system oversight versus product quality assurance.

What are some common challenges faced by a Quality System Manager when implementing new quality standards across an organization?

Quality System Managers often encounter challenges such as resistance to change from staff, aligning new standards with existing processes, and ensuring consistent understanding across departments. Building strong communication channels and providing thorough training are essential to facilitate adoption. Additionally, maintaining regulatory compliance while tailoring the system to the organization's unique needs requires careful planning and collaboration with cross-functional teams.

What are the key skills and qualifications needed to thrive as a Quality System Manager, and why are they important?

To thrive as a Quality System Manager, you need a solid background in quality management principles, regulatory compliance, and process improvement, typically with a degree in engineering, life sciences, or a related field. Familiarity with ISO standards (e.g., ISO 9001), quality management software, and relevant certifications like Six Sigma or ASQ certifications is important. Strong leadership, problem-solving, and communication skills help drive cross-functional initiatives and foster a culture of continuous improvement. These skills ensure effective implementation of quality systems, compliance with industry standards, and sustained operational excellence.

What does a Quality System Manager do?

A Quality System Manager oversees the development, implementation, and maintenance of an organization's quality management systems. They ensure that all processes and products meet established quality standards and comply with relevant regulations. Their responsibilities include auditing processes, managing documentation, training staff on quality procedures, and driving continual improvement initiatives. By monitoring performance and addressing non-conformities, they help organizations deliver consistent, high-quality products or services.
Infographic showing various Quality System Manager job openings in Colorado as of July 2026, with employment types broken down into 83% Full Time, 15% Part Time, 1% Temporary, and 1% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $103,693 per year, or $49.9 per hour.
Quality Assurance Manager

Quality Assurance Manager

Filtration Group Corp

Louisville, CO • On-site

$120K - $140K/yr

Other

Posted 15 days ago


Filtration Group rating

6.6

Company rating: 6.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz


Job description

Overview
Molecular Products makes specialized air-treatment and gas-processing products-basically technology that helps people breathe safely in environments where air is limited or contaminated.
Provides technologies such as CO₂ absorbers, oxygen generators, and activated carbon filters for healthcare, defense, and industrial use.
We are a global leader focused on maintaining safe, breathable air in high-risk and enclosed settings.
Purpose of job
  • To evaluate QMS processes and ensure they are efficient and scalable with the growth of the business for both MPI and OC Lugo businesses.
  • To lead the maintenance and continual improvement of the QMS
  • To lead the effectiveness and compliance of MPI with ISO, ITAR and FDA requirements
  • To lead in the education of staff and ensure their knowledge of the QMS
  • To verify the quality of all products and that all required records are being maintained
Organization
  • The QA Manager will be part of Operations, reporting directly to the Business Unit Leader; any conflicts between Operations and Quality will be addressed through the Group Business Unit Leader.
  • All quality assurance and laboratory personnel will report directly to the QA Manager

Responsibilities
Scope
  • The QA Manager will have the authority to stop any production process if he/she feels that there is any issue with the quality of materials being used or produced. The QA Manager will have the authority to stop any shipments he/she feels do not meet quality requirements until the quality of the shipment can be verified.
  • The QA Manager coordinates the operation of the QA laboratory in order to fulfil its' primary function which is to provide accurate, on-time quality control services to the company and our customers, comply with all standards, keep accurate well organized records, stay aligned with corporate goals, and keep the lab operations in a state to deliver on that mission.
  • The QA Manager will, as necessary, schedule meetings and training sessions with all personnel to insure continued compliance with established quality standards.
  • The QA Manager will oversee the following processes: Internal Auditing, Customer Feedback, Change Orders/Document Control, Non-conforming Material, Deviations, Employee Training, Product Acceptance, Corrective Action and Preventive Actions, and calibration.
  • The QA Manager will establish focus groups and ensure effectiveness of said groups to drive the continuous improvement of the QMS.
  • The QA Manager will oversee the collection and reporting of product trending data to monitor for negative trends and/or process improvements.
  • The QA Manager ensures effective root cause analysis in regards to corrective actions or supplier corrective actions and recommends supplementary actions.
  • The QA Manager will schedule and conduct audits of the QMS to the ISO 9001, ISO 13485, MDSAP standards and ITAR requirements as required, including those requested by customers.
  • The QA Manager in coordination with the Logistics Manager will schedule supplier audits as necessary to insure continued supply of high quality raw materials to MPI.
  • The QA Manager has the authority to approve purchases for supporting QA activities including training, documents, and external testing up to $1000. The QA Manager has the authority to approve purchases for laboratory related expenses up to $1200, including laboratory equipment, repairs, supplies, contract laboratory testing, etc.
Measurement and review
The success of this role will be measured via the delivery of the following:
  • Maintenance of ISO 9001, ISO 13485 and MDSAP registration
  • Effectiveness of the QMS (as evidenced by successful audits)
  • Timely completion of corrective actions
  • Customer Feedback Metrics
  • Awareness and understanding of the QMS and quality standards by all staff
  • Quality Goals as defined by the Management Team
  • Compliance to company policies including EH&S, ITAR and QMS

Qualifications
  • A minimum 5 years of experience in Quality System management
  • A minimum of 5 years experience maintaining an ISO 9001, ISO 13485 and MDSAP QMS
  • A minimum of 3 years experience in conducting audits of an ISO 9001, ISO 13485 and MDSAP system
  • Bachelors degree ideally in Engineering
  • Must demonstrate a working knowledge of ITAR restrictions, Technical Data protection, and restricted visitor protocols.
  • MS Office ¾ Intermediate to Expert knowledge
  • Excellent written and verbal communication skills

Pay: $120,000 - $140,000 USD Annual + 15% annual bonus potential
Location: This position is fully onsite in Louisville CO. Travel once a quarter to the facility in PA.

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