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Quality Engineer Medical Device Jobs in Utah (NOW HIRING)

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Quality Engineer II

Murray, UT · On-site

$67K - $87K/yr

At least 5 years Medical Device quality engineering experience * B.S. in engineering or science * Strong knowledge of FDA QSR and ISO 13485 requirements * Critical thinking and sound decision-making ...

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Quality Engineer Medical Device information

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$33

$64

How much do quality engineer medical device jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for quality engineer medical device in Utah is $33.43, according to ZipRecruiter salary data. Most workers in this role earn between $22.55 and $41.78 per hour, 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 medical devices meet all regulatory standards and quality requirements. They develop and implement quality assurance processes, perform risk assessments, and conduct inspections and audits to make sure products are safe and effective. Quality Engineers also collaborate with design, manufacturing, and regulatory teams to resolve quality issues and improve product reliability. Their work is crucial for maintaining compliance with standards such as ISO 13485 and FDA regulations.

What are the key skills and qualifications needed to thrive as a quality engineer in the medical device industry?

To thrive as a Quality Engineer in the medical device industry, you need a strong background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and engineering principles, often supported by a relevant engineering degree. Familiarity with quality management systems (QMS), risk analysis tools (like FMEA), and certifications such as CQE (Certified Quality Engineer) are typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills and qualifications are vital to maintain regulatory compliance, uphold product quality, and protect patient safety in a highly regulated environment.

How does a quality engineer in the medical device industry typically collaborate with cross-functional teams to ensure product compliance?

Quality Engineers in the medical device sector work closely with cross-functional teams such as design, manufacturing, regulatory affairs, and supply chain. They participate in design reviews, risk assessments, and process validations to ensure that products meet both internal quality standards and external regulatory requirements (such as FDA or ISO 13485). Regular collaboration involves reviewing documentation, addressing non-conformances, and implementing corrective actions. This teamwork is critical to proactively identify potential issues and maintain continuous product quality throughout the development and production lifecycle.

What is the difference between Quality Engineer Medical Device vs Quality Assurance Specialist Medical Device?

AspectQuality Engineer Medical DeviceQuality Assurance Specialist Medical Device
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, Six Sigma, ASQ certifications
Work EnvironmentDesign, development, manufacturing, and process improvementAuditing, compliance, documentation, and process verification
Employer & Industry UsageMedical device manufacturers, R&D labsMedical device companies, regulatory agencies, consulting firms

While both roles focus on quality in the medical device industry, a Quality Engineer Medical Device primarily works on product design, process development, and continuous improvement. In contrast, a Quality Assurance Specialist Medical Device emphasizes compliance, auditing, and ensuring adherence to regulatory standards. Both roles are essential for maintaining product safety and quality, but they differ in scope and daily responsibilities.

More about Quality Engineer Medical Device jobs

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

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

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

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

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

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

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

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

Quality Engineer Medical Device jobs near you
Infographic showing various Quality Engineer Medical Device job openings in Utah as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $69,538 per year, or $33.4 per hour.

Quality Engineer

Stark Pharma Solutions Inc

West Valley City, UT • On-site

$69K - $89K/yr

Contractor

Re-posted 24 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/