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Quality Control Analyst Jobs in Colorado (NOW HIRING)

Raw Materials QC Analyst

Frederick, CO · On-site

$41.27 - $64.48/hr

... QC JOB's. * Reviews data related to all lab testing. * Revises and updates standard operating procedures as needed. * May perform special projects on analytical and instrument problem-solving as time ...

Quality Control Specialist

Monument, CO · On-site

$60K - $65K/yr

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Conduct warranty investigations and root cause analyses to identify failure trends, implement ...

Quality Control Specialist

Monument, CO · On-site

$60K - $65K/yr

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Conduct warranty investigations and root cause analyses to identify failure trends, implement ...

As a Quality Control Specialist, you're the last line of defense between our precision microscopes ... Conduct warranty investigations and root cause analyses to identify failure trends, implement ...

Analyze QC trends, identify deviations, and escalate issues as needed. Participate in root cause investigations and implement corrective/preventive actions (CAPAs). * Maintain accurate and complete ...

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Showing results 1-20

Quality Control Analyst information

See Colorado salary details

$17

$29

$43

How much do quality control analyst jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for quality control analyst in Colorado is $29.35, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $32.60 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst, and why are they important?

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

How much is the salary of a QA analyst?

The salary of a Quality Control Analyst typically ranges from $50,000 to $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. The role often requires knowledge of testing tools and quality assurance processes.

What does a quality control analyst do?

A quality control analyst inspects and tests products or materials to ensure they meet quality standards and specifications. They use testing equipment, follow standard procedures, and document findings to identify defects or issues, often working in manufacturing, pharmaceuticals, or food industries. Attention to detail and knowledge of quality management systems are essential for this role.

What are some common challenges faced by Quality Control Analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What Is a Quality Control Analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

Is QC a high paying job?

Quality Control Analysts typically earn average salaries that are competitive within manufacturing, healthcare, and other industries, with pay often increasing with experience and certifications. While not usually among the highest-paying roles, specialized skills and advanced certifications can lead to higher compensation.

Which pays more, QA or QC?

Quality Control (QC) analysts typically focus on inspecting products and ensuring quality standards, while Quality Assurance (QA) analysts develop processes to prevent defects. Generally, QA roles tend to have higher salaries due to their broader responsibilities and involvement in process improvement, but pay can vary based on industry, experience, and certifications. Both roles are essential in quality management, with QA often commanding higher compensation.
What are the most commonly searched types of Quality Control Analyst jobs in Colorado? The most popular types of Quality Control Analyst jobs in Colorado are:
What are popular job titles related to Quality Control Analyst jobs in Colorado? For Quality Control Analyst jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Quality Control Analyst jobs in Colorado look for? The top searched job categories for Quality Control Analyst jobs in Colorado are:
What cities in Colorado are hiring for Quality Control Analyst jobs? Cities in Colorado with the most Quality Control Analyst job openings:
What are popular job titles related to Quality Control Analyst jobs in CO? For Quality Control Analyst jobs in CO, the most frequently searched job titles are:
Infographic showing various Quality Control Analyst job openings in Colorado as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $61,057 per year, or $29.4 per hour.
QC Analyst II (Onsite) - 1st Shift (Tuesday - Saturday)

QC Analyst II (Onsite) - 1st Shift (Tuesday - Saturday)

Tolmar Inc.

Windsor, CO

$23.75 - $32/hr

Full-time

Posted 11 days ago


Job description

Core Hours: Tuesday - Saturday, 7:00 am - 3:30 pm

  • Training Hours may vary

Purpose and Scope

Performs routine testing of raw materials, cleaning samples, bulk intermediate and finished product, and/or stability samples, according to established regulatory protocols and procedures.

Essential Duties & Responsibilities

  • Perform analyses on a variety of samples using intermediate preparation techniques and analysis methods. Employee will be trained and become proficient in the intermediate preparation techniques and analysis methods.
  • At the direction of management, train junior analysts in analysis methods and lab techniques.
  • Accountable for documenting all activities and maintaining records according to good documentation practices.
  • Accountable for proper use, care and maintenance of instrumentation.
  • Perform intermediate method transfers.
  • Provide detailed accounts of testing performed to investigators. Under the direct supervision of an investigator, may perform investigational testing.
  • Make scientific recommendations to management/technical writers regarding QC procedures.
  • Completes tasks on time and works to eliminate repeat errors. Follows all procedures applicable to job functions to ensure high quality of work.
  • Prioritizes tasks and performs job duties with minimal guidance from management. Works to complete tasks in an efficient manner, and is a productive member of the department. Contributes to a highly productive environment by avoiding distractions.
  • Employee is responsible for ensuring that company and regulatory data integrity guidelines are consistently followed.
  • Accountable for maintaining an atmosphere of teamwork, cordiality and respect towards co-workers. Willing to assist co-workers in the completion of tasks.
  • Will represent the department by providing accounts and results of method transfer activities and assist with troubleshooting aberrant method transfer results, if necessary.
  • Interacts respectfully with all other employees both inside and outside of the department and members of management, and shows interest in others' input and reasoning. Appropriately resolves differences of opinion.
  • Upon delegation, may be responsible for representing the QC chemistry laboratory when communicating with outside departments and vendors.
  • Identifies issues and escalates those issues to the department senior leadership or management as appropriate.
  • Provide support to the department leadership with the implementation of new systems, and continuous improvement efforts. Generates new ideas to create efficiencies and improve processes; willingly supports new ideas and process enhancements.
  • Participate in required annual hazardous waste training. Hazardous waste involvement may include, but is not limited to container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes and transfer of hazardous waste between lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill Procedures.
  • Perform additional duties as assigned.

      Knowledge, Skills & Abilities

      • Knowledge of a government regulated laboratory environment, preferably for drugs or medical devices including cGMP, GLP and ICH and their application to laboratory testing and review processes and procedures.
      • Intermediate understanding of the use of USP, NF and other compendia.
      • Ability to use and maintain analytical laboratory instruments such as HPLC, FTIR, GPC, GC, and UV-Vis spectrophotometers.
      • Effective written and oral communication skills.
      • Knowledge of computer systems for sample tracking, laboratory equipment, raw data handling and storage.
      • Ability to interpret, understand and follow analytical procedures/calculations and scientific principles.

      Core Values

      • The QC Analyst II is expected to operate within the framework of Tolmar’s Core Values:
        • Center on People: We commit to support the well‑being of our patients and treat our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together with an enterprise‑wide mindset that lifts the whole organization.
        • Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
        • Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
        • Constantly Improve: We are committed to a proactive, collaborative effort to enhance our products, systems, processes, and services by reducing waste, increasing efficiency, and improving quality. We strive to be innovative, embracing calculated risk‑taking that drives better ways of working.
        • Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

      Education & Experience

      • Bachelor’s degree in scientific discipline, preferably in Chemistry or Biochemistry.
      • Two or more years of experience in an analytical laboratory position.

      Compensation and Benefits

      • Pay: $36.00 - $37.00 per hour, depending on experience
      • Shift Differential: 10% after training period
      • Benefits summary: https://www.tolmar.com/careers/employee-benefits

      Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

      Working Conditions

      • Laboratory setting. Will be exposed to solvents, bio-hazardous materials, hazardous waste, and pharmaceuticals.
      • Must be adaptable to shifting priorities and operate with a sense of urgency while maintaining high quality in order to meet important timelines in a high throughput lab.
      • Business demands may present a need to work extended hours.

      Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.


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      About Tolmar

      Sourced by ZipRecruiter

      Industry

      Pharmaceutical and medicine manufacturing

      Company size

      1,001 - 5,000 Employees

      Headquarters location

      Fort Collins, CO, US

      Year founded

      2006