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Quality Control Scientist Jobs in Colorado (NOW HIRING)

Agilent

Quality Control Microbiology Analyst

Frederick, CO · On-site

$27.15 - $42.43/hr

Bachelor's of Science (Microbiology, Life Sciences, or related field) * One year of experience in a Quality Control laboratory setting, preferably in the pharmaceutical or biotechnology industry

Actalent

Construction QA/QC

Denver, CO · Hybrid

$80K - $100K/yr

Support mock-up documentation for conveyor system electrical and control device installations ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Tolmar

Sr QC Trainer

Fort Collins, CO · On-site

Provide scientific recommendations to management/technical writers regarding QC procedures as applicable. Complete technical review of applicable procedures. * Complete tasks on time and with minimal ...

Tolmar

Sr QC Trainer

Fort Collins, CO · On-site

Provide scientific recommendations to management/technical writers regarding QC procedures as applicable. Complete technical review of applicable procedures. * Complete tasks on time and with minimal ...

Tolmar Inc.

Sr QC Trainer

Fort Collins, CO · On-site

Provide scientific recommendations to management/technical writers regarding QC procedures as applicable. Complete technical review of applicable procedures. * Complete tasks on time and with minimal ...

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Quality Control Scientist information

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How much do quality control scientist jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for quality control scientist in Colorado is $36.30, according to ZipRecruiter salary data. Most workers in this role earn between $26.06 and $41.73 per hour, depending on experience, location, and employer.

What does a quality control scientist do?

A Quality Control Scientist ensures that products meet required safety, quality, and regulatory standards. They perform laboratory tests, analyze data, and identify deviations in manufacturing processes. Their role is crucial in industries like pharmaceuticals, biotechnology, and food production to maintain compliance and product consistency. They also collaborate with production teams to implement corrective actions and improve quality control procedures.

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

A Quality Control Scientist typically needs a solid background in chemistry, biology, or related sciences, backed by a relevant degree and experience with laboratory testing protocols. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) standards, and analytical instruments such as HPLC or GC is crucial, and certifications like ASQ or Six Sigma can be advantageous. Strong attention to detail, analytical thinking, and effective communication skills help individuals excel in this role. These competencies ensure precise, compliant testing processes and facilitate reliable product quality in regulated industries.

What are some common challenges faced by quality control scientists in their daily work?

Quality Control Scientists often face challenges such as meeting tight production deadlines while maintaining strict adherence to regulatory and quality standards. They must also troubleshoot unexpected test results or equipment issues, which requires patience and analytical problem-solving skills. In addition, collaborating with cross-functional teams, such as manufacturing or R&D, to resolve quality concerns can present communication and coordination challenges. Overcoming these obstacles is essential to ensure that products consistently meet required specifications and industrial regulations.

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

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Quality Control Scientist jobs near you
Infographic showing various Quality Control Scientist job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $75,506 per year, or $36.3 per hour.

Quality Control Microbiology Analyst

Agilent

Frederick, CO • On-site

$27.15 - $42.43/hr

Full-time

Re-posted 9 days ago

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 546 rated manufacturers

Job description

Job Description
The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.
We are seeking a detail-oriented and experienced Quality Control Microbiology Analyst to join our growing Quality team. In this role, you will support product release, stability testing, environmental monitoring, and cleaning verification activities under cGMP and GLP conditions. You'll play a key part in ensuring the quality and safety of pharmaceutical products while maintaining strict compliance with FDA, ICH, and international regulatory standards.
Key Responsibilities
  • Conduct routine and non-routine microbiological and analytical testing in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs)
  • Perform testing for Active Pharmaceutical Ingredients (APIs), final drug products, and in-process samples
  • Review and interpret data to ensure compliance with product specifications; troubleshoot and escalate abnormalities as necessary
  • Conduct environmental monitoring, cleaning verification, and stability testing
  • Ensure laboratory equipment is functioning properly and initiate corrective actions as needed
  • Maintain thorough and accurate documentation following Good Documentation Practices (GDP)
  • Communicate effectively with project managers and internal stakeholders regarding test results, timelines, and any issues
  • Participate in the continuous improvement of laboratory processes, procedures, and quality systems
  • Collaborate cross-functionally to meet project timelines and operational goals

Wednesday-Saturday Shift. 9a.m.-7p.m.
Qualifications
Required:
  • Secondary Education with QC experience
  • Knowledge of analytical equipment and instrumentation

Desired:
  • Bachelor's of Science (Microbiology, Life Sciences, or related field)
  • One year of experience in a Quality Control laboratory setting, preferably in the pharmaceutical or biotechnology industry
  • Knowledge of cGMP guidelines as well as international regulations
  • Knowledge of FDA regulations and guidelines
  • Personal leadership skills and fosters working in a team environment
  • Knowledge of and skills in using computer software and hardware applications, including Microsoft Word and Excel
  • Familiarity with a wide range of microbiological and analytical techniques below is preferred:
    • Bacterial Endotoxin Testing (LAL Analysis)
    • Bioburden Testing (Membrane Filtration)
    • Total Organic Carbon (TOC) Testing
    • Compressed Gas Monitoring
    • Environmental Monitoring
    • UV Analysis
    • USP <61> testing

Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least July 7, 2026 or until the job is no longer posted.
The full-time equivalent pay range for this position is $27.15 - $42.43/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.
Travel Required:
Occasional
Shift:
Day
Duration:
No End Date
Job Function:
Quality/Regulatory

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