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Quality System Manager Jobs in Colorado (NOW HIRING)

Design Quality Engineer III

Boulder, CO · On-site

$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 ...

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 ...

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 ...

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 ...

Hardware Quality Engineer

Centennial, CO · On-site

$123K - $157K/yr

What we don't have is the system that makes inspection credible, repeatable, and scalable. That ... Familiarity with AS9100 or similar quality management frameworks * Experience speccing and ...

What we don't have is the system that makes inspection credible, repeatable, and scalable. That ... Familiarity with AS9100 or similar quality management frameworks * Experience speccing and ...

New

Quality Systems Lead

Longmont, CO · On-site

$80K - $90K/yr

Manages and designs forms, workflows, applications, and analytic dashboards in the Quality Management System (QMS) Cloudtheapp. * Assists in QA management of employee accounts in the QMS * Leads ...

Showing results 21-40

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 Aug 10, 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?

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 August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $103,693 per year, or $49.9 per hour.

Design Quality Engineer III

Collabera

Boulder, CO • On-site

$74K - $96K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 22 days ago


Job description

Company Description

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. 

Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.

Job Description

Design and deliver the medical device and supplies breakthroughs that make a difference in the lives of millions of patients. Responsible for ensuring that software used in the development, manufacturing and as part of medical devices is developed according to good design practices and follows the corresponding requirements set forth by local procedures, regulatory authorities and notified bodies. Provide leadership, oversight and training to division manufacturing plants for computerized system validation. Mentor design teams on quality systems and requirements.

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, defect tracking, configuration management techniques, and knowledge of how these are applied in the software development lifecycle

Experience in Agile software development techniques and IEC 62304 requirements, versed in guidance documents such as TIR-45, IEC TR 80002-1 and Cyber security guidance from FDA

Understanding of current Software Quality techniques, software industry standards (e.g. ISO, IEEE, CMMI), and FDA Quality System Regulations and their impact on internal procedures, software quality, safety and efficacy of products

Experience in risk evaluation techniques, such as Product Risk Assessment and FMEA including software risk assessment and software FMEA

Familiar with reliability analysis and test methods, including software reliability modeling

Working knowledge of C and C++

Good verbal (including presentation) and written communication skills

Ability to effectively work on project teams.


Additional Information

To get further details or to schedule an interview please contact:

Shristi Kshmata

630-315-7388

shristi.kshmata(at)collabera.com