Quality Engineer I

Job Title: Quality Engineer I Job Description
The Quality Engineer I supports a regulated manufacturing environment by performing detailed inspections, developing and improving inspection plans, and analyzing measurement systems to ensure products meet all specifications and quality requirements. This role combines hands-on use of precision measurement equipment with data-driven analysis, engineering drawing interpretation, and quality engineering principles to drive consistent, reliable product quality.
Responsibilities
- Perform incoming inspections and first article inspections to verify product conformance to specifications and quality requirements.
- Conduct dimensional and visual inspections using precision measurement equipment such as calipers, micrometers, height gages, optical comparators, Keyence systems, and other inspection tools.
- Review and interpret engineering drawings, specifications, and Geometric Dimensioning and Tolerancing (GD&T) requirements to determine appropriate inspection methods and acceptance criteria.
- Develop, maintain, and improve inspection plans, sampling plans, inspection procedures, and product acceptance standards to support consistent and efficient quality control.
- Plan, execute, analyze, and document Gage Repeatability and Reproducibility (Gage R&R) studies and other Measurement System Analysis (MSA) activities to assess measurement system capability.
- Evaluate measurement system performance, identify sources of variation, and implement improvements to reduce measurement variation and enhance inspection effectiveness.
- Apply statistical data analysis techniques, using tools such as Minitab or equivalent software, to interpret inspection and measurement data and support quality decisions.
- Support compliance with applicable quality standards, including FDA Quality System Regulations and ISO requirements, by applying quality engineering principles and documented procedures.
- Collaborate with cross-functional teams to communicate inspection results, clarify technical requirements, and resolve quality issues.
- Prepare clear and accurate documentation and reports related to inspections, MSA studies, and quality activities.
- Work independently and as part of a team in a fast-paced, regulated manufacturing environment to meet production and quality objectives.
- Perform other quality-related duties as assigned to support overall quality system effectiveness.
Essential Skills
- Bachelors degree in Engineering or a related technical discipline.
- Approximately 2 years of relevant experience in quality engineering or a similar technical role preferred.
- Hands-on experience planning, executing, analyzing, and documenting Gage R&R and other Measurement System Analysis (MSA) studies.
- Experience conducting statistical data analysis to evaluate measurement systems and product quality.
- Working knowledge of statistical tools and software, including Minitab or equivalent applications.
- Proven experience performing dimensional and visual inspections using precision measurement equipment such as calipers, micrometers, height gages, optical comparators, and Keyence or similar systems.
- Ability to read and interpret engineering drawings, specifications, and Geometric Dimensioning and Tolerancing (GD&T).
- Knowledge of inspection methodologies, sampling plans, and core quality engineering principles.
- Understanding of FDA Quality System Regulations and ISO requirements preferred.
- Strong analytical and problem-solving skills with the ability to identify root causes and propose effective solutions.
- Strong organizational skills with the ability to manage multiple tasks and priorities in a fast-paced environment.
- Excellent written and verbal communication skills with the ability to clearly communicate technical information to diverse audiences.
- Proficiency in Microsoft Office applications, including Excel, Word, and PowerPoint.
Additional Skills & Qualifications
- ASQ Certified Quality Engineer (CQE) certification preferred.
- Prior experience working in a regulated manufacturing environment is highly beneficial.
- Familiarity with ISO-based quality management systems and related documentation practices.
- Demonstrated ability to collaborate effectively with cross-functional teams, including engineering, production, and quality.
- Attention to detail and a commitment to accuracy in measurements, documentation, and data analysis.
- Ability to work both independently with minimal supervision and collaboratively within a team setting.
Work Environment
This position operates within a fast-paced, regulated manufacturing environment where quality and compliance are critical. The role involves frequent use of precision measurement equipment such as calipers, micrometers, height gages, optical comparators, and Keyence or similar inspection systems, as well as regular work with computers and software tools including Minitab and Microsoft Office. Work may take place both at inspection stations on the production floor and in an office or lab setting for data analysis and documentation. The environment emphasizes adherence to established quality procedures, attention to detail, and effective communication across teams to ensure products consistently meet regulatory and customer requirements.
Job Type & Location
This is a Contract position based out of Englewood, CO.
Pay and Benefits
The pay range for this position is $50.00 - $60.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Job Type & Location
This is a Contract position based out of Englewood, CO.
Application Deadline
This position is anticipated to close on Nov 24, 2026.
Workplace Type
This is a fully onsite position in Englewood,CO. About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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sexual orientation, gender identity, genetic information or any characteristic protected
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Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
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It is unlawful in Massachusetts to require or administer a lie detector test as a
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