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Quality Engineer Medical Devices Jobs in Utah (NOW HIRING)

Vector

Manufacturing Quality Engineer

Bluffdale, UT · On-site

$100 - $140/hr

Experience in aerospace, defense, electronics manufacturing, medical devices, or other regulated ... ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt, Six Sigma Black Belt, or equivalent ...

Aerotek

Assembler / Medical Devices

Draper, UT

$19.34/hr

Assembler Of Disposable Medical Devices 1st Shift: Monday-Thursday, 5:30am-4:00pm ($18/hr) 2nd ... quality control. Qualifications: At least 6-12 months of experience in assemble or production ...

Vector

Manufacturing Quality Engineer

Bluffdale, UT · On-site

$71K - $92K/yr

Experience in aerospace, defense, electronics manufacturing, medical devices, or other regulated ... ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt, Six Sigma Black Belt, or equivalent ...

Laborie

Quality Engineer II

Murray, UT · On-site

$67K - $87K/yr

The Quality Engineer II ensures product and process conformity to requirements. Ensuring ... finished medical devices * Perform quality activities in support of Operations ...

Vector

Manufacturing Quality Engineer

Bluffdale, UT · On-site

$71K - $92K/yr

... medical devices, or other regulated industries.Experience with ISO 9001 and/or AS9100 quality ... ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt, Six Sigma Black Belt, or equivalent ...

Quality Electrical Systems

Quality Engineer

West Jordan, UT · On-site

$67K - $86K/yr

Overview The Quality Engineer is responsible for developing, maintaining, and improving Quality Management System (QMS) processes that support the design, manufacturing, testing, and delivery of QES ...

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All JobsQuality Engineer Medical Devices JobsQuality Engineer Medical Devices Jobs in Utah

Quality Engineer Medical Devices information

See Utah salary details

$41K

$76.5K

$108.3K

How much do quality engineer medical devices jobs pay per year?

As of Aug 27, 2026, the average yearly pay for quality engineer medical devices in Utah is $76,507.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $84,700.00 per year, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.

How does a quality engineer collaborate with cross-functional teams in the medical device industry?

Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.

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

To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.

What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?

AspectQuality Engineer Medical DevicesQuality Technician Medical Devices
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, basic quality certifications
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Work EnvironmentDesign and development labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsageMedical device companies, OEMs, suppliersManufacturers, contract labs, quality departments

In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.

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

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

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

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

What cities in Utah are hiring for Quality Engineer Medical Devices jobs?

Cities in Utah with the most Quality Engineer Medical Devices job openings:

Quality Engineer Medical Devices jobs near you
Infographic showing various Quality Engineer Medical Devices 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 $76,507 per year, or $36.8 per hour.

Quality Engineer

West Valley City, UT • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

$69K - $89K/yr

Contractor

Re-posted 4 days ago

Job description

Hi,

My name is Sravani Dasari, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Quality Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows.

Job Title: Quality Engineer
Location: West Valley City, UT
Duration: Long Term

Position Overview

We are seeking an experienced Quality Engineer to support new product development, design quality, and remediation initiatives within a medical device environment. The ideal candidate will possess strong technical expertise in traceability matrix verification (TMV), risk management, verification and validation (V&V), and design integration activities. This role requires hands-on experience developing and executing quality engineering activities while ensuring compliance with applicable regulatory requirements.

Key Responsibilities

• Support new product development and design quality activities throughout the product lifecycle.
• Develop and execute traceability matrix verification (TMV), risk management, and verification & validation (V&V) activities.
• Participate in design integration and design remediation initiatives to ensure product quality and regulatory compliance.
• Support Design History File (DHF) remediation and documentation updates.
• Implement Design for Manufacturing (DFM) principles and support risk management architecture.
• Collaborate with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, and Quality Assurance.
• Ensure compliance with FDA Quality System Regulations and internal quality procedures.
• Contribute to continuous improvement initiatives and quality system enhancements.

Required Qualifications

• Bachelor's Degree in Engineering or a related technical discipline.
• 4+ years of Quality Engineering experience within the medical device industry.
• Experience in New Product Development (NPD) and Design Quality activities.
• Strong knowledge of FDA 21 CFR Part 820 and medical device quality system requirements.
• Hands-on experience developing and executing TMV, Risk Management, and Verification & Validation (V&V) activities.
• Experience with Design Integration, Design Remediation, and Design History File (DHF) remediation.
• Knowledge of Design for Manufacturing (DFM) principles and risk management methodologies.
• Experience with vascular medical devices such as catheters, stents, guidewires, or related products is highly preferred.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/