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Qe Jobs in Colorado (NOW HIRING)

Tolmar

Quality Control Scientist I - NMR

Windsor, CO · On-site

Ensure adherence for compliance with all processes and procedures including training completions, QE and CAPA due dates, notebook and logbook audits, archiving, schedules, internal assessments

Tolmar Inc.

Lab Tech III

Windsor, CO

$18.75 - $25/hr

Ensure adherence for compliance with all processes and procedures including training completions, QE and CAPA due dates, notebook and logbook audits, archiving schedules internal assessments.

BAE Systems

Eng Prin - Quality

Westminster, CO · On-site

$118K - $200K/yr

A demonstrated ability to learn Quality Engineering (QE) principles, tools, methods, and standards. * Must be willing to take initiative, be able to complete tasks in a timely manner, and have good ...

Axos Bank

Software Development Manager

Centennial, CO

$110K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Enforce release governance standards, ensuring all deliverables meet SLA expectations and QE approvals * Lead architecture discussions and modernization initiatives including service isolation ...

BAE Systems

Eng Prin - Quality

Westminster, CO · On-site

$118K - $200K/yr

Expert in Quality Engineering (QE) principles, tools, methods, and standards. * The candidate must demonstrate initiative, be able to complete tasks in a timely manner, possess good interpersonal ...

Tolmar

Lab Tech III

Windsor, CO

$18.75 - $25/hr

Ensure adherence for compliance with all processes and procedures including training completions, QE and CAPA due dates, notebook and logbook audits, archiving schedules internal assessments.

Crusoe

Senior Supervisor, Product Quality

Brighton, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Certified Quality Manager (CQM) or Certified Manager of Quality/Organizational Excellence (CMQ/QE) . * Expertise in ISO 9001 , UL 891 , and Lean Six Sigma tools. * Direct experience developing and ...

Crusoe

Senior Supervisor, Product Quality

Brighton, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Certified Quality Manager (CQM) or Certified Manager of Quality/Organizational Excellence (CMQ/QE) . * Expertise in ISO 9001 , UL 891 , and Lean Six Sigma tools. * Direct experience developing and ...

Fivetran

Staff Software Engineer, Metadata

Denver, CO · On-site

  • Medical

  • PTO

Experience partnering with QE on test strategy and owning operational health - incidents, post-mortems, reliability, and performance * Proficiency in a modern backend or systems language such as ...

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Qe information

See Colorado salary details

$47.3K

$88.4K

$125.1K

How much do qe jobs pay per year?

As of Aug 15, 2026, the average yearly pay for qe in Colorado is $88,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,700.00 and $97,800.00 per year, depending on experience, location, and employer.

What types of projects and teams do quality engineers typically work with?

Quality Engineers often work within multidisciplinary teams that may include design engineers, production staff, and supply chain specialists. Depending on the industry and employer, QEs may be involved in new product development projects, ongoing manufacturing process improvements, or supplier quality management initiatives. They frequently coordinate and lead root cause analyses when defects occur, facilitate audits, and participate in regular meetings to review quality metrics. These collaborative efforts ensure that quality standards are consistently met and that process enhancements are effectively implemented. Working closely with various departments also provides opportunities for professional growth and exposure to different aspects of the business.

What are the key skills and qualifications needed to thrive in the QE position, and why are they important?

To excel as a Quality Engineer (QE), you should have a solid understanding of quality assurance methodologies, statistical analysis, and process improvement, typically backed by a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 9001), root cause analysis tools, and software like Minitab or Six Sigma certifications is highly beneficial. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills in this role. These capabilities are vital for identifying defects, ensuring product consistency, and collaborating with cross-functional teams to drive continuous improvement.

What is a QE?

A QE (Quality Engineer) job focuses on ensuring the quality and reliability of products, software, or processes. Quality Engineers develop and implement testing strategies, identify defects, and work closely with development teams to improve overall product performance. They often use automation, data analysis, and quality standards to streamline testing and enhance efficiency. QEs play a key role in preventing defects rather than just detecting them, helping organizations maintain high-quality standards throughout development.

What are popular job titles related to Qe jobs in Colorado?

For Qe jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Qe jobs in Colorado look for?

The top searched job categories for Qe jobs in Colorado are:

What cities in Colorado are hiring for Qe jobs?

Cities in Colorado with the most Qe job openings:

Qe jobs near you
Infographic showing various Qe job openings in Colorado as of August 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Hybrid job distribution, with an average salary of $88,369 per year, or $42.5 per hour.

Quality Control Scientist I - NMR

Tolmar

Windsor, CO • On-site

Full-time

Re-posted 4 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: Monday - Friday 8:00am - 5:00pm
Purpose and Scope
The Quality Control Scientist I - NMR is a technical leader within the QC functional area with a primary role in scientific development, testing and mentoring of junior analysts. The role is intended for a person with significant pharmaceutical laboratory experience who will contribute product specific scientific knowledge and analytical skills to the QC group.
Essential Duties & Responsibilities
  • Assume a high level, in-depth scientific leadership and mentoring role in the QC laboratory for junior analysts and peers. Such a role may entail training and mentoring of new hires, dissemination of product specific knowledge to the QC group and technical leadership in specific projects as assigned.
  • Conduct complex and challenging QC testing using a variety of instrumentation that needs a high level of analytical technical expertise and in-depth knowledge in chemistry garnered from prior employment experience or academic training.
  • Expert in the analysis, utilization, safety and troubleshooting of NMR instrumentation and NMR method development.
  • Act as a primary technical resource for and be a point of contact for QC and external departments.
  • In depth subject matter expertise in a variety of types of routine instrumentation including NMR, HPLC, GC, FTIR, FTNIR, water content and associated software systems like Chromeleon or Empower.
  • On assignment by management, possesses the ability to resolve testing issues including Out of Specifications and investigations for commercial, stability and developmental samples.
  • Provide scientific recommendations and technical expertise for new instrumentation and methodology that may be introduced in the QCC department.
  • Make scientific recommendations to management and other departments regarding Quality Control laboratory protocols and test procedures. Assist laboratory management in test assignments based on commercial and stability time lines and provide hands-on testing support during commercial exigencies.
  • Assist the departmental leadership in new endeavors including efficiency efforts, organizational tasks, and non-routine activities that require a higher level of scientific skills.
  • Upon delegation, assume a supporting role to the management team on activities such as the issuance of COA's, review of Change controls, test methods and specifications.
  • Provide support to the QC department for the evaluation and implementation of new technological innovations in laboratory automation systems, documentation systems and other technologies.
  • Perform change assessments and change controls for changes in testing, documents and specifications.
  • Validate and install new laboratory instrumentation systems including development of new test methods for the associated instrumentation.
  • Serve as a project team member and collaborate with CORE teams throughout the development lifecycle.
  • Prioritize workload to meet timelines while ensuring on-time delivery of all projects, testing and action items.
  • Take ownership of tasks and results from initiation to completion to meet commitments and proactively address outcomes.
  • Escalate and communicate items that arise per the timelines specified in the department escalation strategy.
  • Execute all business and department goals and initiatives on time.
  • Support and execute all potential 3-day field alert investigations and actions expeditiously.
  • Submit document change requests for all document updates and minimize document revisions for routine updates where possible
  • Identify, and complete cost savings initiatives and facilitate continuous improvement.
  • Participate in leadership development activities and take an active role during department and company activities
  • Participate on project teams, company and department meetings, third party audits, and regulatory audits.
  • Demonstrate leadership aptitude in technical functions
  • Ability to perform designated duties under minimal supervision and support departmental management in all aspects of organizational functions
  • Ensure adherence for compliance with all processes and procedures including training completions, QE and CAPA due dates, notebook and logbook audits, archiving, schedules, internal assessments
  • Accountable for maintaining a positive atmosphere of teamwork, camaraderie and respect towards co-workers.
  • Participates 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 CP 030-0202 Chemical Spill Response.
  • Perform various other duties as assigned.

Knowledge, Skills & Abilities
  • Expert knowledge of NMR instrumentation and data analysis.
  • A demonstrated knowledge of fundamental chemistry pertaining to specific products and assays conducted in the Tolmar QC laboratory.
  • Possesses a strong sense of purpose and drive to meet deadlines without sacrificing quality.
  • Balances the need for speed with a commitment to accuracy and quality, completing tasks thoughtfully and effectively
  • Knowledge in analytical method validation and instrument qualification
  • Expert knowledge in analytical testing of drug substances and formulations for Chemistry or Microbiology
  • Thorough knowledge of government regulations of drugs and medical devices as they apply to laboratory work
  • Ability to grasp and enhance the technical expertise required for new products in the pipeline in order to support QC functions as per business needs.
  • High level of proficiency in Quality Control laboratory procedures and testing techniques.
  • Hands-on, operational and troubleshooting knowledge of analytical instrumentation within the QC department. Ability to evaluate and adapt new technologies that are to be introduced to the department based on business needs.
  • Knowledge of analytical troubleshooting and product investigation
  • Expert knowledge of cGMP practices, regulatory and ICH guidelines.
  • An excellent grasp on USP and other compendial methods.
  • Proficient in the use of analytical laboratory instruments such as HPLC, FTIR, GPC, GC, and UV-Vis spectrophotometers, CCIT, plate readers, and MODA.
  • Ability to prepare, review, conduct and assess analytical method validations, feasibility and suitable for use.
  • Knowledge of computer applications including Microsoft Office.
  • Experience in authoring technical reports.
  • Excellent oral and written communication skills demonstrated through interactions internally and externally.
  • Ability to manage multiple projects concurrently and under tight time constraints.

Core Values
This position 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
  • Previous in depth NMR testing and troubleshooting experience is required.
  • BS, MS or PhD in Chemistry, Biochemistry, Pharmaceutical Sciences or related field.
  • BS combined with 10 or more years Pharmaceutical cGMP laboratory work: Masters combined with 8 or more years Pharmaceutical cGMP laboratory work: or PhD: and 5 or more years Pharmaceutical cGMP laboratory work.
  • Experience in the pharmaceutical industry to include experience with cGMP analytical testing of drug substances (DS) and Drug products (DP), preferably in high-volume Quality Control laboratory required.

Working Conditions
  • Working conditions are typical for an office environment in addition to a laboratory setting to include exposure 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
  • Annual pay range $115,000 - $125,000 depending on experience
  • Bonus Eligible
  • Benefits information: 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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