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Qc Quality Control Jobs in Colorado (NOW HIRING)

STAQ Pharma Inc

Quality Control Technician

Denver, CO · On-site

$24/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Quality Control Technician supports the QC function in a 503B pharmaceutical manufacturing environment by helping ensure materials, samples, documentation, and environmental monitoring activities ...

Blackstone Consulting Inc.

Experience * Minimum three years related Food Service/Quality Control experience with a major culinary institution, a large institutional food service operation or the military. General ...

University of Colorado

Quality Control Supervisor

Aurora, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Supervisor Position #: 00828303 - Requisition #:40538 Job Summary: This position is a full-time, supervisor-level position for the Quality Control (QC) team at the Gates ...

University of Colorado

Quality Control Supervisor

Aurora, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Supervisor Position #: 00828303 - Requisition #:40538 Job Summary: This position is a full-time, supervisor-level position for the Quality Control (QC) team at the Gates ...

Haselden Construction

Quality Control Manager

Centennial, CO · On-site

$95K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Quality Control Manager is responsible for implementing Haselden's Quality Control Program across assigned projects. This position partners with project teams, subcontractors, consultants, and ...

Epicurean Butter

Quality Control Supervisor

Thornton, CO · On-site

$24 - $30/hr

Quality Control Technician Supervisor Department: QA Direct Supervisor/Manager: Director of Quality Assurance Backup Employee: Director of Quality Assurance General Scheduled hours for this position ...

Tolmar Inc.

Quality Control Planner

Fort Collins, CO

$19.25 - $26.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC laboratory. This position will coordinate and communicate across QC and other departments to organize ...

Tolmar

Quality Control Planner

Fort Collins, CO · On-site

$19.25 - $26.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC laboratory. This position will coordinate and communicate across QC and other departments to organize ...

Tolmar

Quality Control Planner

Fort Collins, CO · On-site

$39 - $40.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC laboratory. This position will coordinate and communicate across QC and other departments to organize ...

TotalEnergies

QC Chemist

Grand Junction, CO · On-site

The QC Chemist is responsible for maintaining the Quality Control Laboratory at the Grand Junction Plant and ensuring products meet customer quality requirements through comprehensive quality control ...

New

QUIKRETE Companies

Quality Control Technician

Silverthorne, CO · On-site

$18.75 - $24.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As a Quality Control Technician with Quikrete Heavy Construction Materials you will be responsible for ensuring quality control of batching, mixing, and delivering high-quality ready-mixed concrete ...

QUIKRETE Companies

Quality Control Technician

Grand Junction, CO · On-site

$18.25 - $23.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a QUALITY CONTROL TECHNICIAN in Grand Junction , CO . As a Quality Control Technician with Quikrete Heavy Construction Materials you will be responsible for ensuring quality ...

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All JobsQc Quality Control JobsQc Quality Control Jobs in Colorado

Qc Quality Control information

What is the difference between Qc Quality Control vs Quality Assurance?

AspectQc Quality ControlQuality Assurance
Primary FocusInspecting products and identifying defectsPreventing defects through process improvements
CertificationsOften requires certifications like ASQ CQE or CQASimilar certifications, emphasizing process management
Work EnvironmentManufacturing, production lines, labsQuality management systems, audits, process reviews
Industry UsageManufacturing, construction, pharmaceuticalsManufacturing, software, service industries

While both roles aim to ensure product quality, Qc Quality Control focuses on inspecting and testing products for defects, whereas Quality Assurance emphasizes establishing processes to prevent defects from occurring. Both roles often require similar certifications and are integral to quality management in various industries.

Do you need a degree for Qc Quality Control?

A degree is not always required for a Quality Control (QC) role, but many employers prefer candidates with a high school diploma or equivalent, along with relevant technical training or certifications. Skills in inspection, attention to detail, and knowledge of industry standards are often more important than formal education for QC positions.

Is QA QC a good career?

Quality Control (QC) and Quality Assurance (QA) roles are essential in manufacturing, construction, and software industries, focusing on maintaining product standards and process improvements. These careers often require attention to detail, technical skills, and certifications such as Six Sigma or ISO standards, and can offer stable employment with opportunities for advancement.

Is QC quality control a high paying job?

Quality Control (QC) roles can offer competitive salaries depending on industry, experience, and location. Entry-level positions typically pay around minimum wage to moderate salaries, while experienced QC inspectors or managers in specialized fields can earn higher wages, often supplemented by certifications and overtime opportunities.

What is the job of quality control (QC)?

A Quality Control (QC) professional is responsible for inspecting and testing products or materials to ensure they meet specified quality standards. They identify defects, document issues, and work with production teams to improve processes, often using tools like measurement instruments and quality management systems. QC roles require attention to detail and knowledge of industry standards and certifications.

What are popular job titles related to Qc Quality Control jobs in Colorado?

For Qc Quality Control jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Qc Quality Control jobs in Colorado look for?

The top searched job categories for Qc Quality Control jobs in Colorado are:

What cities in Colorado are hiring for Qc Quality Control jobs?

Cities in Colorado with the most Qc Quality Control job openings:

Qc Quality Control jobs near you
Infographic showing various Qc Quality Control 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.

Quality Control Technician

STAQ Pharma Inc

Denver, CO • On-site

$24/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago

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