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Quality System Jobs in Colorado (NOW HIRING)

TDA Research

Senior Quality Engineer

Golden, CO · On-site

$95K - $140K/yr

QMS Implementation and Management -- Serve as the Quality System Management Representative; deploy and maintain a right‑sized QMS aligned with ISO 13485, ISO 14971 and other relevant regulatory ...

TDA Research

Senior Quality Engineer

Golden, CO · On-site

$95K - $140K/yr

QMS Implementation and Management - Serve as the Quality System Management Representative; deploy and maintain a right-sized QMS aligned with ISO 13485, ISO 14971 and other relevant regulatory ...

Injectech LLC

Quality Manager

Fort Collins, CO · On-site

$90K - $115K/yr

Maintain and continuously improve the electronic Quality Management System (eQMS), quality documentation, and controlled records in accordance with ISO 13485. * Ensure compliance with ISO 13485 ...

Injectech LLC

Quality Manager

Fort Collins, CO · On-site

Maintain and continuously improve the electronic Quality Management System (eQMS), quality documentation, and controlled records in accordance with ISO 13485. * Ensure compliance with ISO 13485 ...

trane technologies

Manufacturing Quality Engineer

Pueblo, CO · On-site

$73K - $94K/yr

This role will effectively administer the Quality Management System and focus on Execution of Process Quality as per Advanced Product Quality Planning (APQP) requirements in accordance with current ...

Philips

Supplier Quality Engineer

Colorado Springs, CO · On-site

$63K - $100K/yr

Job TitleSupplier Quality Engineer The Supplier Quality Engineer supports supplier qualification ... Executes MSA (Measurement System Analysis), PFMEA (Process Failure Mode and Effects Analysis ...

Philips

Supplier Quality Engineer

Colorado Springs, CO · On-site

$63K - $100K/yr

Job Title Supplier Quality Engineer The Supplier Quality Engineer supports supplier qualification ... Executes MSA (Measurement System Analysis), PFMEA (Process Failure Mode and Effects Analysis ...

New Generation Wellness

Be Seen First

Quality Assurance Supervisor

Colorado Springs, CO · On-site

$60K - $80K/yr (+ commission)

This role ensures compliance with FDA regulations, internal SOPs, and quality-system requirements while fostering a proactive, collaborative quality culture. Reporting to the Quality Manager, the QA ...

Agile Space Industries

Quality Engineer II/III

Durango, CO · On-site

$80K - $120K/yr

At Agile, we design, build, and test in-space propulsion systems that give spacecraft the ability ... Quality Engineer II The Quality Engineer II is responsible for supporting compliance with quality ...

Agile Space Industries

Quality Engineer II/III

Durango, CO · On-site

$80K - $120K/yr

At Agile, we design, build, and test in-space propulsion systems that give spacecraft the ability ... Quality Engineer II The Quality Engineer II is responsible for supporting compliance with quality ...

Medtronic

Sr Design Quality Engineer

Lafayette, CO · On-site

$92K - $124K/yr

Ensure design changes are executed in accordance with Medtronic's Quality Management System (QMS) and applicable global regulations including ISO 13485, EU MDR, and FDA Quality System Regulation (21 ...

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Quality System information

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How much do quality system jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality system in Colorado is $26.96, according to ZipRecruiter salary data. Most workers in this role earn between $23.51 and $30.34 per hour, depending on experience, location, and employer.

What is a quality system?

Quality System jobs involve developing, implementing, and maintaining the processes and standards that ensure a company’s products or services meet regulatory and customer requirements. Professionals in these roles often work with quality management systems (QMS), conduct audits, and ensure compliance with industry regulations like ISO standards. They play a key role in continuous improvement by identifying areas for enhancement and working with other teams to resolve quality-related issues. Quality System jobs are vital across industries such as manufacturing, healthcare, and pharmaceuticals to guarantee product safety, reliability, and effectiveness.

What skills and qualifications are needed to thrive as a quality systems specialist?

To thrive as a Quality Systems Specialist, you need a strong understanding of quality management principles, regulatory standards (such as ISO 9001), and typically a degree in engineering, life sciences, or a related field. Familiarity with quality management software (QMS), document control systems, and relevant certifications like Six Sigma or ASQ are commonly required. Attention to detail, problem-solving abilities, and strong communication skills help ensure compliance and continuous improvement. These skills are essential to maintain product quality, meet regulatory requirements, and support organizational excellence.

What are common challenges faced by professionals working in quality systems, and how can they be addressed?

Professionals in Quality Systems often encounter challenges such as ensuring compliance with evolving regulatory standards, maintaining thorough documentation, and fostering a culture of continuous improvement across departments. Addressing these challenges typically involves staying updated on industry regulations, implementing effective training programs, and utilizing robust digital tools for document management. Additionally, strong communication and collaboration with cross-functional teams are essential to align quality objectives with broader organizational goals.

What is the difference between Quality System vs Quality Assurance?

AspectQuality SystemQuality Assurance
DefinitionFramework of policies, processes, and procedures to ensure quality management across an organization.Part of the quality system focused on preventing defects through planned activities and systematic processes.
FocusOverall quality management and compliancePreventing defects and ensuring product/service quality
CertificationsISO 9001, QS-9000ISO 9001, Six Sigma, CQA
Work EnvironmentCross-departmental, organizational-wideSpecific to quality processes and audits

In summary, a Quality System encompasses the entire framework for managing quality within an organization, including policies and procedures. Quality Assurance is a key component of the Quality System, focusing specifically on preventing defects and ensuring quality through systematic activities.

What are the most commonly searched types of Quality System jobs in Colorado?

The most popular types of Quality System jobs in Colorado are:

Quality System jobs near you
Infographic showing various Quality System job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $56,073 per year, or $27 per hour.

Quality Senior Engineer I - Englewood, CO - Onsite

Englewood, CO • On-site

Fusion Life Sciences
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Fusion Life Sciencesexternal

$87K - $118K/yr

Contractor

Re-posted 21 days ago

Job description

 
Job Title: Quality Senior Engineer I
Location: Englewood, CO - Onsite
Duration: 12 Months
 
Duties

·Review, remediate, and migrate legacy CAPA records into EtQ to ensure completeness, accuracy, and compliance with global procedures.

·Manage assigned CAPAs through initiation, investigation support, action tracking, effectiveness verification, and closure.

·Perform gap assessments of CAPA records and support correction of documentation deficiencies to meet regulatory and internal quality system requirements.

·Partner cross-functionally with Quality, Regulatory, Operations, and Engineering to support CAPA execution and remediation activities.

·Support compliance to global CAPA procedures, including documentation standards, timeliness expectations, and record retention requirements.

·Assist with training and user guidance related to CAPA procedures and EtQ processes.

Skills

·Working knowledge of CAPA processes, root cause analysis, and quality system requirements.

·Experience with electronic Quality Management Systems (EtQ preferred).

·Knowledge of applicable regulations and standards, including 21 CFR Part 820, ISO 13485, and risk-based quality principles.

·Strong technical writing and documentation review skills.

·Strong organizational skills with high attention to detail and ability to manage multiple priorities.

·Analytical/problem-solving skills with ability to identify gaps and drive resolution.

·Ability to work cross-functionally and communicate effectively across levels of the organization.

·Proficiency with Microsoft Office (Excel, Word, PowerPoint) and document control systems.

·Medical device or other regulated industry experience preferred.

 

Education

B.S. in engineering or an alternative Bachelor’s degree program

3-5 years of experience required in a Quality Engineering role, preferably supporting CAPA processes

Knowledge of FDA QSR (21 CFR 820), ISO 13485, and ISO 14971 preferred.

Knowledge of design controls, risk management, FMEA, CAPA, root cause investigation and statistical analysis.

Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred