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Semiconductor Quality Engineer Jobs in Utah (NOW HIRING)

Navitas Semiconductor

$96K - $130K/yr

Navitas Semiconductor (Nasdaq: NVTS) is a next-generation power semiconductor leader driving ... Test Engineering (test strategy, cost drivers, yield improvement) * Ensure procurement is embedded ...

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Senior Consulting Engineer

Midvale, UT · On-site

$120K - $160K/yr

... empower semiconductor manufacturers to achieve unprecedented levels of efficiency, quality, and ... The consulting engineer must be a highly motivated and self-driven team player with strong ...

PDF Solutions

Senior Consulting Engineer

Midvale, UT · On-site

$120K - $160K/yr

... empower semiconductor manufacturers to achieve unprecedented levels of efficiency, quality, and ... The consulting engineer must be a highly motivated and self-driven team player with strong ...

Texas Instruments

Photo Process Engineer

Lehi, UT · On-site

Join the Revolution in Semiconductor Manufacturing at LFAB! We're at the forefront of an exciting ... operations, and product quality * Implement project or improvement plans for areas of ...

Texas Instruments

Photo Process Engineer

Lehi, UT · On-site

Join the Revolution in Semiconductor Manufacturing at LFAB! We're at the forefront of an exciting ... operations, and product quality * Implement project or improvement plans for areas of ...

Navitas Semiconductor

Partner with Product Engineering, Device Engineering, Test Engineering, Quality, Supply Chain ... Proven experience developing and releasing power semiconductor modules from concept and prototype ...

Navitas Semiconductor

Navitas Semiconductor (Nasdaq: NVTS) is a next-generation power semiconductor leader driving ... Drive action item closure across engineering, supply chain, quality, and foundry/OSAT teams ...

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Semiconductor Quality Engineer information

What does a semiconductor quality engineer do?

A Semiconductor Quality Engineer is responsible for ensuring that semiconductor products meet established quality standards and specifications. They develop and implement quality control processes, perform failure analysis, and collaborate with engineering and manufacturing teams to resolve quality issues. Their work includes analyzing data, conducting audits, and driving continuous improvement in production processes to minimize defects and ensure product reliability. Ultimately, they play a crucial role in guaranteeing that semiconductor devices are safe and perform as intended for end users.

What are some common challenges semiconductor quality engineers face in ensuring product reliability?

Semiconductor Quality Engineers often encounter challenges related to rapidly evolving manufacturing processes, stringent industry standards, and the need to detect minute defects that can impact chip performance. They must work closely with cross-functional teams, including design, process, and production engineers, to implement robust quality controls and root cause analyses. Staying updated on new technologies and maintaining clear communication are essential for managing quality issues efficiently and ensuring that products meet both customer and regulatory expectations.

What are the key skills and qualifications needed to thrive as a semiconductor quality engineer, and why are they important?

To thrive as a Semiconductor Quality Engineer, you need expertise in quality assurance, semiconductor manufacturing processes, and statistical analysis, usually supported by a degree in engineering or a related field. Familiarity with tools such as Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), and quality management systems like ISO 9001 is typically required. Strong problem-solving abilities, attention to detail, and effective communication skills set outstanding candidates apart. These competencies are essential to ensure product reliability, maintain industry standards, and drive continuous improvement in semiconductor manufacturing.

What is the difference between Semiconductor Quality Engineer vs Semiconductor Process Engineer?

AspectSemiconductor Quality EngineerSemiconductor Process Engineer
Primary FocusEnsuring product quality, defect prevention, and compliance with standardsDesigning, developing, and optimizing manufacturing processes
Skills & CertificationsQuality management, testing, inspection, certifications (e.g., ISO)Process engineering, manufacturing techniques, statistical analysis
Work EnvironmentQuality labs, manufacturing floors, supplier auditsCleanrooms, fabrication facilities, process development labs
Industry UsageUsed across semiconductor manufacturing companies focusing on product qualityUsed in process development and manufacturing optimization

The Semiconductor Quality Engineer primarily focuses on maintaining and improving product quality, ensuring standards are met, and preventing defects. In contrast, the Semiconductor Process Engineer concentrates on developing and refining manufacturing processes to enhance efficiency and yield. Both roles are essential in semiconductor manufacturing but serve different aspects of the production cycle.

What are popular job titles related to Semiconductor Quality Engineer jobs in Utah?

For Semiconductor Quality Engineer jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Semiconductor Quality Engineer jobs in Utah look for?

The top searched job categories for Semiconductor Quality Engineer jobs in Utah are:

What cities in Utah are hiring for Semiconductor Quality Engineer jobs?

Cities in Utah with the most Semiconductor Quality Engineer job openings:

Semiconductor Quality Engineer jobs near you
Infographic showing various Semiconductor Quality Engineer job openings in Utah as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Quality Engineer II - Process Engineering

Edwards Lifesciences Corporation

Salt Lake City, UT • On-site

$69K - $90K/yr

Full-time

Posted 29 days ago

Edwards Lifesciences rating

8.2

Company rating: 8.2 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

86th of 545 rated manufacturers

Job description

Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You'll bring your passion for problem solving and partner with various teams to influence decision-making for a product's entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.
The Quality Engineer II will support the PASCAL Gen 3 product line at our Draper facility, partnering closely with manufacturing, supplier quality, and cross-functional engineering teams to stabilize a new product line, improve yield, resolve quality issues, and help prepare for future product launches. Your work will help ensure commercially released and human-use products continue to meet rigorous quality expectations while directly impacting patients around the world. The Quality Engineer II will also be a part of next-generation process development.
You will make an impact by:
  • Supporting sustaining Quality Engineering activities for the PASCAL Gen 3 product line, including stabilization of a new product line, commercial part number support, and continuous improvement of manufacturing quality performance.
  • Utilizing learnings from current generation sustaining to develop and launch the next generation PASCAL products
  • Partnering with Manufacturing Engineering, Supplier Quality Engineering, Operations, and other cross-functional partners to identify quality trends, improve yield, and drive metrics-based improvements across the production line.
  • Owning or supporting nonconformance activities, including NCR authoring, investigations, dispositions, containment, corrective actions, NCR reductions, and related documentation in accordance with quality system requirements.
  • Developing, executing, reviewing, and approving engineering studies, test method validations, and manufacturing process validation deliverables, with emphasis on TMVs and OQ/PQ protocol and report review.
  • Creating, optimizing, and sustaining dimensional inspection routines, including Keyence programming or similar optical/automated inspection methods used to support manufacturing and human-use product requirements.
  • Applying engineering and quality tools such as root cause analysis, risk assessment, FMEAs, statistical methods, Lean/Six Sigma, and structured problem solving to improve process capability and reduce manufacturing risk.
  • Providing technical feedback to supplier quality partners regarding supplier-related quality issues, inspection approaches, material performance, and opportunities to improve incoming or in-process quality.
  • Developing, updating, and maintaining technical documentation, work instructions, validation documentation, risk documentation, and training materials to ensure effective production support and knowledge transfer.
  • Collaborating with technicians, inspectors, engineers, and production teams by assigning support tasks, providing technical guidance, reviewing test work, and helping reinforce quality expectations on the manufacturing floor.

What you'll need (Required):
  • Bachelor's degree in engineering or scientific field with two (2) years of Quality Engineering or Manufacturing Engineering experience in a production, manufacturing, or operations environment; OR Master's degree in engineering or scientific field with no experience (or applicable internship/co-op experience).
  • Experience supporting production line sustaining activities.
  • Experience working in a highly regulated industry such as medical device, aerospace, automotive, semiconductor, or a similarly regulated manufacturing environment.

What else we look for (Preferred):
  • Medical device industry experience.
  • Hands-on NCR authoring experience, including investigation, disposition, root cause analysis, corrective action, and documentation closure.
  • Keyence programming experience or experience creating/sustaining optical dimensional inspection routines using similar automated inspection technology.
  • Experience with process validations and test method validations, including protocol execution, report writing, and review of Test Method Validation and OQ/PQ documentation.
  • Experience with FMEAs, risk management documentation, root cause analysis, CAPA support, investigations, and quality improvement initiatives.
  • Working knowledge of quality systems, manufacturing documentation, engineering change control, investigations, and compliance expectations.
  • Ability to use data, metrics, and statistical techniques to identify trends, improve yield, reduce defects, and support manufacturing decision-making.
  • Strong documentation, communication, and interpersonal skills with the ability to partner effectively across cross-functional teams.
  • Strong problem-solving, organizational, analytical, and critical thinking skills with strict attention to detail.
  • Ability to manage competing priorities in a fast-paced production environment.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

What Edwards Lifesciences employees say

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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958

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