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Medical Device Engineer Jobs in Utah (NOW HIRING)

Ambition 24Hours Inc

Senior Manager ft

Salt Lake City, UT · On-site

$165K - $188K/yr

Ensure compliance with medical device standards and regulatory requirements REQUIREMENTS * PhD in Chemical Engineering, Chemistry, Biomedical Engineering (Materials Focus), or related scientific ...

SPECTRUM PLASTICS MASTER

Tooling Engineer II

Sandy, UT · On-site

Bachelor's degree (BA/BS) in Mechanical Engineering, Chemical Engineering, Materials Science, or a ... A minimum of three (3) years of experience in medical device manufacturing and/or extrusion or ...

Spectrum Plastics Group

Tooling Engineer II

Sandy, UT · On-site

$70 - $110/hr

Bachelor's degree (BA/BS) in Mechanical Engineering, Chemical Engineering, Materials Science, or a ... A minimum of three (3) years of experience in medical device manufacturing and/or extrusion or ...

Spectrum Plastics Group

Tooling Engineer II

Sandy, UT · On-site

Bachelor's degree (BA/BS) in Mechanical Engineering, Chemical Engineering, Materials Science, or a ... A minimum of three (3) years of experience in medical device manufacturing and/or extrusion or ...

Varex Imaging

CAPA Process Lead

Salt Lake City, UT · On-site

At least five years of quality assurance, quality engineering, or quality systems experience in the medical device industry, including direct hands-on responsibility for CAPA investigations and ...

Vareximaging

CAPA Process Lead

Salt Lake City, UT · On-site

At least five years of quality assurance, quality engineering, or quality systems experience in the medical device industry, including direct hands-on responsibility for CAPA investigations and ...

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Medical Device Engineer information

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$19

$45

$87

How much do medical device engineer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical device engineer in Utah is $45.37, according to ZipRecruiter salary data. Most workers in this role earn between $31.97 and $54.28 per hour, depending on experience, location, and employer.

What does a medical device engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What does a medical device engineer do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

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

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What are some common challenges medical device engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

More about Medical Device Engineer jobs

What are the most commonly searched types of Medical Device Engineer jobs in Utah?

The most popular types of Medical Device Engineer jobs in Utah are:

What are popular job titles related to Medical Device Engineer jobs in Utah?

For Medical Device Engineer jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Medical Device Engineer jobs in Utah look for?

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Cities in Utah with the most Medical Device Engineer job openings:

What are popular job titles related to Medical Device Engineer jobs in UT?

For Medical Device Engineer jobs in UT, the most frequently searched job titles are:

Medical Device Engineer jobs near you
Infographic showing various Medical Device Engineer job openings in Utah as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 22% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $94,371 per year, or $45.4 per hour.

Quality Engineer II - Process Engineering

Edwards Lifesciences Corporation

Salt Lake City, UT • On-site

$69K - $90K/yr

Full-time

Posted 19 days ago

Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

67th of 544 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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Benefits

Hours and flexibility

Workplace

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Edwards Lifesciences logo

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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