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Fulltime Quality Control Inspector Jobs in Denver, CO

STAQ Pharma Inc

Quality Control Technician

Denver, CO · On-site

$24/hr

Perform sampling and inspection of in-process and finished products according to approved ... At STAQ Pharma, all full time employees have access to: * Medical, dental, and vision insurance ...

Ryan Companies

Quality Control Manager

Denver, CO · On-site

Set quality management expectations, including the quantity and timing of field inspections ... Monitor, Track, Log and Audit all quality control activities, including all testing, inspections ...

STAQ Pharma Inc

Quality Control Manager

Denver, CO · On-site

$120K/yr

The QC Manager will encourage and motivate associates to be successful and focused on Safety ... Participates in internal/external audits and regulatory inspections. * Supports the stability ...

STAQ Pharma Inc

Quality Control Manager

Denver, CO · On-site

$120K/yr

The QC Manager will encourage and motivate associates to be successful and focused on Safety ... Participates in internal/external audits and regulatory inspections. * Supports the stability ...

TAK Broadband

Quality Control Technician

Denver, CO · On-site

$20 - $24/hr

Job Type Full-time Description TAK Broadband is a leading end-to-end U.S. fiber broadband network ... You will perform inspections post-install to ensure compliance to client specifications and ...

Elevation Labs

QC Tech

Denver, CO · On-site

$22 - $25/hr

Auditing and inspection on raw materials, components, sub-assembly, in-process, and finish goods to ... Quality Control Experience preferably in personal care or related industry.Experience working in a ...

Elevation Labs

QC Tech

Denver, CO · On-site

$22 - $25/hr

Auditing and inspection on raw materials, components, sub-assembly, in-process, and finish goods to ... Quality Control Experience preferably in personal care or related industry. * Experience working in ...

Elevation Labs LLC

QC Tech

Denver, CO · On-site

$22 - $25/hr

Auditing and inspection on raw materials, components, sub-assembly, in-process, and finish goods to ... Quality Control Experience preferably in personal care or related industry. * Experience working in ...

Eurofins

Quality Control Specialist

Centennial, CO · On-site

Participates in quality audits or regulatory inspections. * Assist with the validation and ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options

TAK Broadband

Quality Control Technician

Denver, CO · On-site

$20 - $24/hr

You will perform inspections post-install to ensure compliance to client specifications and ... Why TAK? * Full Time * Paid Weekly * Compensation: $20 - $24 per hour, DOE * Full Benefits Package ...

TAK Broadband

Quality Control Technician

Denver, CO · On-site

$20 - $24/hr

You will perform inspections post-install to ensure compliance to client specifications and ... Why TAK? * Full Time * Paid Weekly * Compensation: $20 - $24 per hour, DOE * Full Benefits Package ...

Verstela

Quality Control Technician

Centennial, CO · On-site

$24/hr

This full-time temporary opportunity offers paid training, a clean work environment and high probability of conversion to regular hire. Quality Control Technician Job Duties * Perform environmental ...

Brannan Companies

Quality Control Technician

Denver, CO · On-site

$22 - $24/hr

Quality Control Manager FLSA Status: Full Time Location: Denver Area Plant and Jobsite Locations Position Summary : This position involves the performance and record keeping for quality control tests ...

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All JobsFulltime Quality Control Inspector JobsFulltime Quality Control Inspector Jobs in Denver, CO

Fulltime Quality Control Inspector information

See Denver, CO salary details

$12

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How much do fulltime quality control inspector jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for fulltime quality control inspector in Denver, CO is $22.10, according to ZipRecruiter salary data. Most workers in this role earn between $17.84 and $24.76 per hour, depending on experience, location, and employer.

What is the difference between Fulltime Quality Control Inspector vs Quality Assurance Technician?

AspectFulltime Quality Control InspectorQuality Assurance Technician
CertificationsOften requires quality control certifications (e.g., CQI, ISO auditor)May require similar certifications, with additional focus on QA methodologies
Work EnvironmentPrimarily on-site inspection in manufacturing or production facilitiesOn-site and office settings, involved in process audits and documentation
Industry UsageCommon in manufacturing, automotive, aerospace industriesUsed across manufacturing, pharmaceuticals, and food industries
Job FocusInspecting products for defects, ensuring quality standardsDeveloping and implementing quality systems, process improvements

While both roles focus on quality, the Fulltime Quality Control Inspector primarily conducts product inspections on-site, whereas the Quality Assurance Technician emphasizes developing quality systems and process improvements. Both roles often require similar certifications and are vital in manufacturing industries.

How do you become a fulltime quality control inspector?

To become a full-time quality control inspector, candidates typically need a high school diploma or equivalent, along with relevant experience or training in quality assurance or manufacturing. Certifications such as ASQ Certified Quality Inspector can improve job prospects, and strong attention to detail, analytical skills, and familiarity with inspection tools are important for success.

How much do fulltime quality control inspectors earn?

Fulltime quality control inspectors typically earn a median annual salary of around $40,000 to $50,000, depending on experience, industry, and location. Salaries can range from approximately $30,000 for entry-level positions to over $60,000 for experienced inspectors or those with specialized skills and certifications.

Is fulltime quality control inspector a good career?

A fulltime quality control inspector is a stable career that involves inspecting products to ensure they meet quality standards, often requiring attention to detail and knowledge of industry regulations. The role can offer steady employment, opportunities for advancement, and sometimes certifications like Six Sigma or ISO standards. Job prospects depend on the industry and location, with manufacturing and production sectors typically offering the most opportunities.

What are popular job titles related to Fulltime Quality Control Inspector jobs in Denver, CO?

For Fulltime Quality Control Inspector jobs in Denver, CO, the most frequently searched job titles are:

What job categories do people searching Fulltime Quality Control Inspector jobs in Denver, CO look for?

The top searched job categories for Fulltime Quality Control Inspector jobs in Denver, CO are:

Fulltime Quality Control Inspector jobs near you

Quality Control Technician

STAQ Pharma Inc

Denver, CO • On-site

$24/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted just now

Key responsibilities

  • Coordinate QC sample preparation and shipment/submission of samples to external laboratories for testing activities.

  • Assist with environmental monitoring and microbiological sample evaluation activities, including organizing samples and reviewing forms.

  • Perform sampling and inspection of in-process and finished products according to approved procedures and quality expectations.

Job description


Position Summary:

The Quality Control Technician supports the QC function in a 503B pharmaceutical manufacturing environment by helping ensure materials, samples, documentation, and environmental monitoring activities are handled in accordance with cGMP, company procedures, and applicable regulatory requirements. This role provides hands-on support across QC, QA, and Operations, including coordinating QC sample preparation, external laboratory submissions, environmental monitoring support, retention material management, raw material and sterile supply release support, and review of GMP documentation. The QC Technician plays an important role in patient safety by helping verify that materials, environments, samples, and records meet quality expectations before they support manufacturing or product release.

What This Role Does Day-to-Day:

In this role, the QC Technician may support incoming material review, retention sample organization, sample preparation, environmental monitoring sample coordination, third-party laboratory submissions, biohazard waste coordination, logbook generation, GMP document review, and inspection activities for in-process or finished product samples. Daily work may include preparing and tracking samples, verifying documentation, using vendor portals or paper submissions for external testing, reviewing room and equipment logs, assisting with investigations, and communicating quality data or concerns to department leadership. The role requires strong attention to detail, accurate documentation, comfort working in or around cleanroom environments, and the ability to escalate issues that may impact product quality, compliance, or patient safety.

Key Responsibilities:

  • Coordinate QC sample preparation and shipment/submission of samples to external laboratories for environmental monitoring, microbiological, raw material, in-process, finished product, and other required testing activities.
  • Use third-party laboratory web portals, paper submission forms, and internal tracking tools to support accurate sample submission, chain-of-custody, and follow-up on required testing.
  • Assist with environmental monitoring and microbiological sample evaluation activities, including organizing samples, reviewing forms, and escalating missing, incomplete, or questionable information.
  • Maintain retention materials, including organization, tracking, storage support, and disposal when required by procedure.
  • Assist with review and release support for raw materials, APIs, excipients, sterile supplies, and other incoming materials as assigned.
  • Perform sampling and inspection of in-process and finished products according to approved procedures, sampling plans, and quality expectations.
  • Coordinate biohazard waste destruction activities in accordance with internal procedures and safety requirements.
  • Generate, issue, organize, or maintain logbooks and controlled documents as assigned.
  • Review GMP documents, including production environmental monitoring forms, room logs, equipment logs, sample forms, and related quality records for accuracy, completeness, and GDP expectations.
  • Support investigations, deviations, CAPAs, and continuous improvement activities by gathering information, reviewing documentation, and helping identify appropriate corrective or preventive actions.
  • Support quality management system activities, including document control, training program support, and cross-functional quality initiatives.
  • Work closely with Production, QA, QC, Warehouse, and external laboratory vendors to support timely sample flow, material review, documentation accuracy, and quality communication.
  • Identify and escalate potential documentation errors, sample discrepancies, environmental monitoring concerns, material issues, or process deviations to the appropriate quality leadership.
  • Follow all applicable cGMP, GDP, SOP, OSHA, FDA, and company policy requirements.
  • Perform other duties as assigned based on business and quality needs.

What Success Looks Like: 

  • Maintains accurate, organized, and traceable QC records, sample documentation, logbooks, and submission information.
  • Understands that sample handling, environmental monitoring support, and documentation accuracy directly impact patient safety and product quality.
  • Follows procedures carefully and asks for clarification before proceeding when information is unclear or does not match expectations.
  • Communicates clearly with QC, QA, Production, Warehouse, and third-party laboratories to keep quality activities moving forward.
  • Identifies and escalates quality concerns, missing documentation, sample discrepancies, or potential deviations in a timely manner.
  • Balances urgency with compliance and does not sacrifice accuracy, documentation, or safety to move work faster.
  • Demonstrates strong attention to detail, professionalism, reliability, and a willingness to learn within a regulated manufacturing environment.
  • Supports continuous improvement by identifying opportunities to improve sample tracking, documentation flow, communication, and quality processes.

Required Qualifications:

  • Associate degree in the sciences or equivalent experience preferred.
  • At least 1 year of Quality Control Technician experience preferred.
  • Pharmaceutical, medical device, biotechnology, laboratory, sterile manufacturing, or regulated manufacturing experience preferred.
  • Familiarity with cGMP, GDP, FDA-regulated environments, quality documentation, or controlled procedures preferred.
  • Strong attention to detail and ability to review records, forms, and logs for completeness and accuracy.
  • Excellent written, verbal, interpersonal, and independent judgment skills.
  • Ability to work in a fast-paced environment with changing priorities, competing deadlines, and cross-functional requests.
  • Proficiency with Microsoft Word, Excel, PowerPoint, Outlook, and ability to learn vendor portals or internal quality systems.
  • Must be able to speak, read, and write in English.
  • Must be a team player with a professional, quality-focused, and patient-safety mindset.

Physical Requirements: 

  • Ability to work in or around cleanroom and controlled manufacturing environments as required.
  • Ability to wear required PPE and follow gowning, cleanliness, and safety procedures.
  • Prolonged periods of sitting at a desk and working on a computer.
  • Ability to stand, walk, bend, reach, and handle samples, materials, or documentation as needed.
  • Ability to lift up to 15 pounds at times.

Work Environment: 

This position supports QC activities within a 503B pharmaceutical manufacturing environment and may involve work in cleanroom, controlled, laboratory support, warehouse, and office settings. Employees are expected to follow all applicable PPE, gowning, cleanliness, documentation, safety, and quality requirements. The role requires regular interaction with production areas, quality records, samples, materials, external laboratories, and cross-functional teams.

Benefits:

We offer a comprehensive and competitive benefits package designed to support the health, well-being, and financial security of our employees and their families.

At STAQ Pharma, all full time employees have access to:

  • Medical, dental, and vision insurance options
  • Employer-paid life insurance and disability coverage
  • Employee Assistance Program
  • 401(k) retirement plan with employer match
  • Paid time off (PTO), sick leave  
  • 7 paid holidays
  • Opportunities for professional growth in a regulated pharmaceutical manufacturing environment
  • Employee-focused culture emphasizing safety, quality, and teamwork


The application window for this position is anticipated to be open at least 25 days