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Senior Quality Control Inspector Jobs in Denver, CO

STAQ Pharma Inc

Quality Control Technician

Denver, CO · On-site

$24/hr

The Quality Control Technician supports the QC function in a 503B pharmaceutical manufacturing ... Perform sampling and inspection of in-process and finished products according to approved ...

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

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

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 ...

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 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 ...

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 ...

Eurofins

Quality Control Specialist

Centennial, CO · On-site

Analyze QC trends, identify deviations, and escalate issues as needed. Participate in root cause ... Participates in quality audits or regulatory inspections. * Assist with the validation and ...

Freshpoint

Quality Control Associate

Denver, CO · On-site

$19.09 - $28.61/hr

... product quality control. RESPONSIBILITIES Provide technical, customer relations, and personnel ... Inspect inbound freight, warehoused product, and/or outbound product and document product condition ...

Beehive Industries

Senior Quality Engineer

Centennial, CO · On-site

$110K - $136K/yr

Role Overview The Senior Quality Engineer role will monitor and improve the quality of Beehive ... Developing and implementing quality control systems in an R&D/Production environment * Monitoring ...

Crusoe

Mechanical Quality Inspector

Brighton, CO · On-site

Incoming Quality Control (IQC): Inspect raw materials, structural steel, and sub-assemblies upon arrival against purchase orders, engineering specs, drawings, supplier CoCs (Certificate of Compliance ...

Crusoe

Mechanical Quality Inspector

Brighton, CO · On-site

Incoming Quality Control (IQC): Inspect raw materials, structural steel, and sub-assemblies upon arrival against purchase orders, engineering specs, drawings, supplier CoCs (Certificate of Compliance ...

MKS Instruments, Inc.

Sr Quality Engineer

Broomfield, CO · On-site

$88K - $147K/yr

As a Sr Quality Engineer at MKS, you will partner with Operations, Engineering, and Internal Teams ... Performing analysis and identifying trends in inspection data. Using statistical analysis tools to ...

MKS Instruments, Inc.

Sr Quality Engineer

Broomfield, CO

$88K - $147K/yr

As a Sr Quality Engineer at MKS, you will partner with Operations, Engineering, and Internal Teams ... Developing quality data collection plans and inspection/process documentation. Performing analysis ...

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Senior Quality Control Inspector information

See Denver, CO salary details

$17

$34

$49

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

As of Sep 2, 2026, the average hourly pay for senior quality control inspector in Denver, CO is $34.45, according to ZipRecruiter salary data. Most workers in this role earn between $27.31 and $40.96 per hour, depending on experience, location, and employer.

What does a senior quality control inspector do?

A Senior Quality Control Inspector is responsible for overseeing the inspection and testing of products or materials to ensure they meet established quality standards and specifications. They lead inspection teams, develop and implement testing procedures, and document inspection outcomes. Senior QC Inspectors also identify defects, recommend improvements, and may train junior inspectors. They play a critical role in maintaining product quality, safety, and compliance with industry regulations.

What are the key skills and qualifications needed to thrive as a senior quality control inspector?

To excel as a Senior Quality Control Inspector, you need a solid background in quality assurance, knowledge of inspection techniques, and familiarity with industry standards, often supported by relevant certifications such as ASQ or Six Sigma. Proficiency in using measuring instruments, statistical process control (SPC) software, and documentation systems is typically required. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for ensuring compliance and mentoring junior inspectors. These competencies are essential for maintaining product quality, minimizing defects, and supporting continuous improvement in manufacturing or production environments.

What are some typical challenges faced by senior quality control inspectors, and how can they be addressed?

Senior Quality Control Inspectors often encounter challenges such as keeping up with evolving industry standards, managing tight production schedules, and ensuring consistent compliance across teams. Addressing these challenges typically involves proactive communication with production staff, ongoing training on new regulations, and effective use of quality management systems. Building strong relationships with both junior inspectors and production teams can also help to identify issues early and foster a culture of continuous improvement.

What is the difference between Senior Quality Control Inspector vs Quality Control Inspector?

AspectSenior Quality Control InspectorQuality Control Inspector
CertificationsISO, ASQ certifications often preferredBasic quality assurance certifications may be required
Work EnvironmentManufacturing plants, laboratories, construction sitesManufacturing facilities, production lines
ResponsibilitiesOversees inspection processes, mentors staff, reviews reportsPerforms inspections, documents findings, ensures compliance
ExperienceTypically 3+ years in quality control rolesEntry to mid-level experience

The Senior Quality Control Inspector generally has more experience, leadership duties, and advanced certifications compared to a Quality Control Inspector. Both roles work in similar environments within manufacturing or construction industries, but the senior position involves oversight and mentorship responsibilities.

How much do senior quality control inspectors earn?

Senior quality control inspectors typically earn between $60,000 and $85,000 annually, depending on experience, industry, and location. They often have certifications such as ASQ CQI and use tools like inspection gauges and testing equipment to ensure product quality.

What are the most commonly searched types of Quality Control Inspector jobs in Denver, CO?

The most popular types of Quality Control Inspector jobs in Denver, CO are:

What cities near Denver, CO are hiring for Senior Quality Control Inspector jobs?

Cities near Denver, CO with the most Senior Quality Control Inspector job openings:

Infographic showing various Senior Quality Control Inspector job openings in Denver, CO as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 5% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $72,715 per year, or $35 per hour.

Quality Control Technician

STAQ Pharma Inc

Denver, CO • On-site

$24/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 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