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Qa Document Control Associate Jobs in Denver, CO

CesiumAstro

Quality Assurance Associate

Westminster, CO · On-site

$83K - $99K/yr

Execute quality control processes per purchased product, manufacturing operations, and customer ... Document inspection activities using electronic systems, written logs, and labels. * Assist with ...

Honeywell

Sr Document Control Coordinator

Arvada, CO · On-site

$25.48 - $31.82/hr

... quality, and compliance. Your role supports various departments and maintains document control ... YOU MUST HAVE Associate's degree or equivalent experience preferred 8+ years of experience in ...

CesiumAstro

Quality Assurance Associate

Westminster, CO · On-site

$83K - $99K/yr

Execute quality control processes per purchased product, manufacturing operations, and customer ... Document inspection activities using electronic systems, written logs, and labels. * Assist with ...

Actalent

Construction QA/QC

Denver, CO · Hybrid

$80K - $100K/yr

Quality Assurance Specialist - Electrical Engineer We are seeking a dedicated Electrical Engineer ... Support mock-up documentation for conveyor system electrical and control device installations.

STAQ Pharma Inc

Quality Control Technician

Denver, CO · On-site

$24/hr

This role provides hands-on support across QC, QA, and Operations, including coordinating QC sample ... documentation flow, communication, and quality processes. Required Qualifications: * Associate ...

TekWissen

Document Control Coordinator

Westminster, CO · On-site

Maintain Device Master Records and Device History Records as well as other quality system documents such as training records, monitoring records, authorized signature lists, etc. Qualifications One ...

CRAZY SHIRTS

Quality Assurance

Aurora, CO

$19.29/hr

Physically performs all inspections as documented on all inspection criteria and specifications ... Participates routinely in product processing and quality control inspections as part of the Product ...

Crazy Shirts

Quality Assurance

Aurora, CO · On-site

$19.29/hr

Physically performs all inspections as documented on all inspection criteria and specifications ... Participates routinely in product processing and quality control inspections as part of the Product ...

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All JobsQa Document Control Associate JobsQa Document Control Associate Jobs in Denver, CO

Qa Document Control Associate information

See Denver, CO salary details

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How much do qa document control associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for qa document control associate in Denver, CO is $27.26, according to ZipRecruiter salary data. Most workers in this role earn between $19.04 and $34.62 per hour, depending on experience, location, and employer.

What is a QA Document Control Associate?

QA Document Control Associates are professionals responsible for managing, organizing, and maintaining documentation related to quality assurance (QA) processes within an organization. Their duties often include ensuring that all documents comply with regulatory standards, are properly stored, and are easily accessible for audits or inspections. They play a crucial role in supporting quality systems by controlling document revisions, distribution, and archiving to maintain accuracy and compliance. This role is essential in industries like pharmaceuticals, biotechnology, and manufacturing where precise documentation is required by law or industry standards.

What are the key skills and qualifications needed to thrive as a QA Document Control Associate?

To thrive as a QA Document Control Associate, you need strong attention to detail, organizational skills, and a foundational understanding of quality assurance principles, often supported by a degree in a scientific or technical field. Familiarity with document management systems (DMS), regulatory compliance software, and standards such as ISO 9001 is typically required. Excellent communication, problem-solving abilities, and a proactive mindset are standout soft skills in this role. These competencies ensure accurate documentation, regulatory compliance, and efficient quality processes crucial to organizational success.

What are some common challenges faced by a QA Document Control Associate, and how can they be managed effectively?

QA Document Control Associates often encounter challenges such as managing large volumes of documents, ensuring version control, and meeting strict regulatory compliance deadlines. Staying organized through robust document management systems and maintaining clear communication with cross-functional teams are key strategies for success. Regular training on industry regulations and utilizing checklists can also help prevent errors and maintain document integrity. Proactivity and attention to detail are especially important in this role, as even small oversights can have significant impacts on audits and quality assurance processes.

What is the difference between Qa Document Control Associate vs Quality Assurance Specialist?

AspectQa Document Control AssociateQuality Assurance Specialist
CredentialsTypically requires a high school diploma or associate degree; certifications like ISO or document control training are commonRequires a bachelor's degree in a related field; certifications such as ASQ CQE or CQA are often preferred
Work EnvironmentOffice and document management settings within manufacturing, pharmaceutical, or biotech industriesQuality labs, manufacturing sites, or office environments focused on product quality and compliance
Employer & Industry UsageUsed by companies needing document control for quality systems in regulated industriesUsed by organizations ensuring product quality, compliance, and process improvements

The Qa Document Control Associate primarily manages and maintains quality documentation, ensuring compliance and proper record keeping. In contrast, the Quality Assurance Specialist focuses on evaluating and improving quality processes and product standards. Both roles are essential in regulated industries but differ in scope and responsibilities.

Qa Document Control Associate jobs near you
Infographic showing various Qa Document Control Associate job openings in Denver, CO as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 21% Part Time, 4% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $56,703 per year, or $27.3 per hour.

Quality Assurance Associate

CesiumAstro

Westminster, CO • On-site

$83K - $99K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 5 days ago

Job description

Please Note: To conform with the United States Government Space Technology Export Regulations, the applicant must be a U.S. citizen, lawful permanent resident of the U.S., conditional resident, asylee or refugee (protected individuals as defined by 8 U.S.C. 1324b(a)(3)), or eligible to obtain the required authorizations from the U.S. Department of State.
At CesiumAstro, we are developers and pioneers of out-of-the-box communication systems for satellites, UAVs, launch vehicles, and other space and airborne platforms. We take pride in our dynamic and cross-functional work environment, which allows us to learn, develop, and engage across our organization. If you are looking for hands-on, interactive, and autonomous work, CesiumAstro is the place for you. We are actively seeking passionate, collaborative, energetic, and forward-thinking individuals to join our team.
We are looking to add a Quality Assurance Associate to our team. In this position, you will work closely on an integrated team of CesiumAstro managers, engineers, and other cross-functional personnel. You will be responsible for programming and using inspection/analysis equipment, handling nonconformances and corrective actions, calibration and metrology of equipment, as well as performing inspections on electronic assemblies and finished high reliability products in compliance with CesiumAstro Quality Management System, international standards, and regulatory requirements.
JOB DUTIES AND RESPONSIBILITIES
  • Execute quality control processes per purchased product, manufacturing operations, and customer quality requirements.
  • Inspect parts, assemblies, and finished products utilizing necessary tools and equipment in accordance with approved procedures, specifications, and drawings.
  • Perform measurements using calipers, height gauges, thread gauges, and CMM/VMM equipment.
  • Document inspection activities using electronic systems, written logs, and labels.
  • Assist with the control and disposition of non-conforming material (MRB).
  • Drive scheduling of day-to-day quality activities and ensure timely and accurate turnaround of inspection and quality processes.
  • Program, maintain, and utilize automated inspection equipment such as CMMs, inspection arms, XRF systems, X-Ray equipment, and automated visual inspection systems.
  • Perform calibration of equipment and tools used in Quality, Production, and Test activities.
  • Create, document, and update quality processes related to inspection, measurement system analysis (MSA), calibration, and data analysis.
  • Assist in the development, maintenance, and continuous improvement of inspection methods, inspection plans, internal quality procedures, and quality processes.
  • Drive resolution of internal and external nonconformances utilizing root cause analysis, corrective action, and 8D methodologies.
  • Lead cross-functional teams to identify issues, implement corrective actions, and drive continuous improvement efforts.
  • Conduct data analysis and department metrics reporting to support quality objectives and operational decision-making.
  • Assist in the resolution of audit findings, observations, and recommendations resulting from internal, customer, and regulatory audits.
  • Perform other quality control duties and special projects as assigned.

JOB REQUIREMENTS AND MINIMUM QUALIFICATIONS
  • 5-7 years of experience in manufacturing quality, metrology, and failure analysis.
  • Associate degree in a technical field preferred. High school diploma or equivalent.
  • Experience in the aerospace, electronics, or defense industry.
  • Experience with Coordinate Measuring Machines (CMM), metrology arms, Keyence systems, or similar inspection and measurement equipment.
  • Experience with calibration systems and metrology practices preferred.
  • Experience with AS9100 or ISO 9001 Quality Management Systems.
  • Proficiency reading engineering drawings, CAD models, GD&T, specifications, and detailed work instructions.
  • Experience with microscopic visual inspection.
  • Strong attention to detail and ability to follow procedures, specifications, and work instructions.
  • Strong analytical, written, verbal, and digital communication skills.
  • Strong interpersonal skills and ability to work collaboratively with cross-functional teams.

PREFERRED EXPERIENCE
  • Experience in regulated manufacturing environments such as aerospace, defense, automotive, or medical device industries.
  • J-STD-001, IPC-A-610, and/or IPC/WHMA-A-620 certification.

$83,000 - $99,000 a year
CesiumAstro considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. Full-time employment offers include company stock options and a generous benefits package including health, dental, vision, HSA, FSA, life, disability and retirement plans.
CesiumAstro is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
Please note: CesiumAstro does not accept unsolicited resumes from contract agencies or search firms. Any unsolicited resumes submitted to our website or to CesiumAstro team members will be considered property of CesiumAstro, and we will not be obligated to pay any referral fees.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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