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Senior Quality Control Analyst Jobs in Colorado (NOW HIRING)

Senior Quality Engineer

Englewood, CO · On-site

$95K - $121K/yr

The Senior Quality Engineer plays a critical role in ensuring that products and processes meet the ... Experience with statistical process control (SPC) and data analysis software. Preferred ...

Compri Consulting is seeking a Sr. QA Analyst for a 7-month contract with our client in Boulder, CO. No C2C/third party candidates are able to be considered at this time. * 4+ years of Software QA ...

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Senior Quality Control Analyst information

See Colorado salary details

$15

$51

$71

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

As of Aug 15, 2026, the average hourly pay for senior quality control analyst in Colorado is $51.02, according to ZipRecruiter salary data. Most workers in this role earn between $44.47 and $57.12 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior quality control analyst, and why are they important?

To thrive as a Senior Quality Control Analyst, you need expertise in laboratory testing, analytical methods, and a strong understanding of regulatory standards, often supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), chromatography software, and relevant certifications such as GMP training are typically required. Attention to detail, strong problem-solving abilities, and effective communication skills distinguish top performers in this role. These competencies ensure accurate quality assessments, compliance with regulations, and efficient collaboration across teams to maintain product integrity.

How much does a senior quality control analyst earn?

A senior quality control analyst typically earns between $70,000 and $100,000 annually, depending on experience, industry, and location. They often have certifications such as CQE and use tools like laboratory testing equipment, with some roles requiring overtime or shift work.

What are some common challenges faced by senior quality control analysts, and how are they typically addressed?

Senior Quality Control Analysts often encounter challenges such as managing tight deadlines while maintaining high accuracy, adapting to evolving regulatory standards, and troubleshooting unexpected deviations in product quality. These challenges are typically addressed through effective collaboration with cross-functional teams, ongoing professional development to stay updated with industry regulations, and implementing robust standard operating procedures. Additionally, strong analytical and communication skills help in swiftly resolving issues and ensuring continuous improvement within the quality control process.

What does a senior quality control analyst do?

A Senior Quality Control Analyst is responsible for overseeing and ensuring the quality of products or processes within a company, typically in industries like pharmaceuticals, manufacturing, or food production. They design and implement testing procedures, analyze data, identify defects or inconsistencies, and ensure compliance with regulatory standards. Additionally, they mentor junior analysts, prepare reports, and collaborate with other departments to improve quality systems. Their expertise helps maintain product integrity and supports continuous improvement initiatives.

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 Senior Quality Control Analyst jobs in Colorado?

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

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

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

What cities in Colorado are hiring for Senior Quality Control Analyst jobs?

Cities in Colorado with the most Senior Quality Control Analyst job openings:

Infographic showing various Senior Quality Control Analyst job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $106,115 per year, or $51 per hour.

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

Tolmar Inc.

Fort Collins, CO • On-site

$23.50 - $31.50/hr

Full-time

Posted 11 days ago


Tolmar rating

9.8

Company rating: 9.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

1st of 86 rated pharmaceutical


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.


      What Tolmar employees say

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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