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Senior Quality Control Analyst Jobs in Colorado (NOW HIRING)

Corden Pharma Colorado

QC Analyst

Boulder, CO · On-site

$31.65 - $39/hr

Analytical skills and knowledge of general or organic chemistry * Mechanical aptitude with lab ... Support Senior level QC staff with general lab duties * Preform basic methods on test samples

Tolmar Inc.

Sr QC Trainer

Fort Collins, CO · On-site

Mentor analysts in day to day testing and documentation after training to ensure they are ... The Senior QC Trainer is expected to operate within the framework of Tolmar's Core Values: * Center ...

Tolmar

Sr QC Trainer

Fort Collins, CO · On-site

Mentor analysts in day to day testing and documentation after training to ensure they are ... The Senior QC Trainer is expected to operate within the framework of Tolmar's Core Values: * Center ...

Tolmar

Sr QC Trainer

Fort Collins, CO

Mentor analysts in day to day testing and documentation after training to ensure they are ... The Senior QC Trainer is expected to operate within the framework of Tolmar's Core Values: * Center ...

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Senior Quality Control Analyst information

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

As of Aug 22, 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 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 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 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.

What is the role of a senior quality control analyst?

A senior quality control analyst is responsible for inspecting and testing products or materials to ensure they meet quality standards and regulatory requirements. They analyze data, identify issues, and collaborate with production teams to improve processes, often using tools like laboratory equipment and quality management systems. This role typically requires experience, attention to detail, and knowledge of industry-specific regulations.

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:

Senior Quality Control Analyst jobs near you
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, 13% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $106,115 per year, or $51 per hour.

Senior QC Analyst (2nd Shift; Tues - Sat)

Tolmar

Fort Collins, CO • On-site

$47 - $50/hr

Full-time

Re-posted 21 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, 3:00 pm - 11:30 pm
- Training hours may vary
Purpose and Scope
Performs complex testing of raw materials, bulk intermediate and finished products, and stability samples, according to established regulatory protocols and procedures, in support of manufacturing.
Essential Duties & Responsibilities
  • Expertise in performing analyses on a variety of samples using advanced preparation techniques and analysis methods. Expertise with basic and intermediate techniques and analysis methods.
  • Provide mentorship to QC analyst in all aspects of analyses performed within the QC chemistry laboratory including but not limited to documentation, procedures, and regulations.
  • Accountable for documenting all activities and maintaining records according to good documentation practices.
  • Accountable for proper use, care, maintenance, and troubleshooting of instrumentation.
  • Performs high-level method transfers. Guides the department in the evaluation and implementation of new technologies.
  • Provide detailed accounts of testing performed to investigators. Perform investigational testing as directed by a primary investigator.
  • Perform laboratory investigations with management assistance.
  • Make scientific recommendations to management/technical writers regarding QC procedures. Able to take recommendations and incorporate those recommendations into a document to ensure the appropriate changes are made.
  • Responsible for acting as a technical reviewer for document updates to ensure changes that are made are justified and scientifically sound.
  • Route documents in the electronic document control system to ensure document updates are routed promptly and correctly.
  • Act as a subject matter expert for the QC department.
  • Complete tasks on time and with minimal errors. Follow all procedures applicable to job functions to ensure high quality of work. Mentor others in the department to ensure department maintains high standards for quality of work.
  • Prioritize tasks and performs job duties with minimal guidance from management.
  • Contributes to a highly productive environment by avoiding distractions.
  • Responsible for ensuring that company and regulatory data integrity guidelines are consistently followed.
  • Participates in required monthly safety trainings and annual HAZ-COM, RCRA and API handling trainings. Hazardous waste involvement may include but is not limited to making waste determinations, generation, transportation, satellite accumulation, storage and disposal of multiple types of waste streams, and container management and inspections. Respond to spills per company procedures. Maintain compliance to all Tolmar health and safety policies, as well as OSHA standards.
  • Accountable for maintaining an atmosphere of teamwork, cordiality and respect towards co-workers. Exhibits a positive and understanding attitude at all times. Remembers to look at situations from all aspects. Assists co-workers with the completion of tasks. Able to identify areas of contention on the team and will work with QC management to correct.
  • Support adherence to department budget by identifying alternative cost-saving and compliant materials and equipment, where appropriate.
  • Represent the department by providing accounts and results of method transfer activities and assist with troubleshooting aberrant method transfer results, if necessary. May provide technical expertise to determine root cause of aberrant method transfer results.
  • Interact 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.
  • A leader in compliance. Lead implementation of change and escalates issues as necessary. Demonstrate leadership aptitude in technical functions.
  • Identify issues and possible solutions and escalates those issues and solutions 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.
  • Understand and process complex information and exercises sound judgment, considering the situation, the issues, the key players and the levels of authority involved. Propose courses of action that further the objectives, priorities, and vision of the organization; sees "big picture".
  • Perform additional duties as assigned.

Core Values
The Sr. QC Analyst 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. We are committed to treating 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.
  • 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 collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.
  • 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.

Knowledge, Skills & Abilities
  • Advanced knowledge and application of government regulations for drugs or medical devices including GMP, GLP and ICH and their application to laboratory testing and review processes and procedures.
  • Advanced knowledge in the use of USP, NF and other compendia.
  • Highly proficient use of analytical laboratory instruments such as HPLC, FTIR, GPC, GC, and UV-Vis spectrophotometers.
  • Knowledge of computer systems for sample tracking, laboratory equipment, raw data handling and storage.
  • Effective written and oral communication skills.
  • Ability to interpret, understand and follow analytical procedures and calculations.
  • Demonstration of training and project leadership skills.
  • Ability to train analysts on complex methodology.
  • Expert knowledge in analytical testing of drug substances and formulations.

Education & Experience
  • Bachelor's degree in scientific discipline, preferably in Chemistry or Biochemistry.
  • Six or more years of experience in an analytical laboratory position using advanced techniques and demonstrated proficiency with complex testing.

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.

Compensation and Benefits
  • Pay: $47.00 - $50.00 depending on experience
  • Shift differential: 18%
  • 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.
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.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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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

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