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Medical Device Engineer Jobs in Logan, UT (NOW HIRING)

Sogeti

Mechancial Engineer

Mendon, UT · On-site

We are seeking a Mechanical Engineer to support the design and development of automated mobile ... Medical, Prescription, Dental & Vision Insurance * Life Insurance * 100% Company-Paid Mobile Phone ...

KBR

Quality Engineer

Logan, UT · On-site

$62K - $80K/yr

Quality Engineer BELONG. CONNECT. GROW. with KBR. Around here, we define the future. We are a ... with company match, medical, dental, vision, life insurance, AD&D, flexible spending account ...

Spartronics LLC

Product Engineer - Mid Level

Logan, UT · On-site

$80K - $95K/yr

Here, you'll have the opportunity to work with industry leaders in Aerospace & Defense, Medical ... We are seeking a passionate and driven Product Engineer to join our growing team. In this role, you ...

Spartronics LLC

Product Engineer - Mid Level

Logan, UT · On-site

$80K - $95K/yr

Spartronics- Product Engineer Location: North Logan, UT Work Schedule: On-site | Monday through ... Here, you'll have the opportunity to work with industry leaders in Aerospace & Defense, Medical ...

Autonomous Solutions

Perception Engineer IV

Mendon, UT · On-site

$100 - $130/hr

JOB SUMMARY The Perception Engineer IV develops and advances perception systems that enable ASI ... ASI covers 90% of employee medical plan costs At Autonomous Solutions, Inc. (ASI), we are committed ...

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Showing results 21-40

All JobsMedical Device Engineer JobsMedical Device Engineer Jobs in Logan, UT

Medical Device Engineer information

See Logan, UT salary details

$18

$42

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How much do medical device engineer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for medical device engineer in Logan, UT is $42.93, according to ZipRecruiter salary data. Most workers in this role earn between $30.24 and $51.35 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.

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Medical Device Engineer jobs near you
Infographic showing various Medical Device Engineer job openings in Logan, UT as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $89,296 per year, or $42.9 per hour.

Regulatory Affairs Specialist

ELITechGroup Inc.

Logan, UT • On-site

Full-time

Re-posted 8 days ago

Job description

SummaryThis role is responsible for ensuring that all products comply with applicable global regulatory requirements throughout their lifecycle-from development and registration to post-market surveillance. The Regulatory Affairs Specialist helps ensure regulatory compliance for diagnostics products with FDA, Health Canada, EU, other regulatory bodies, ISO, and business objectives.Essential Duties and Responsibilities Implement company regulatory affairs procedures.Prepare, compile, and submit regulatory documentation (e.g., 510(k), PMA, CE Technical Files) to global regulatory agencies and with guidance from Regulatory Affairs Manager manage regulatory submissions.Interpret and apply FDA, EU MDR, ISO 13485, and other international regulations to ensure product compliance.Collaborate with cross-functional teams (R&D, Quality, Clinical, Marketing) to support product development and regulatory strategy.Review and approve product labeling, instructions for use (IFUs), and promotional materials for regulatory compliance.Monitor and analyze changes in regulatory requirements and communicate updates to internal stakeholders.Support internal and external audits, including FDA inspections and Notified Body assessments.Maintain regulatory files and databases, ensuring accurate and up-to-date documentation.Participate in post-market surveillance activities, including adverse event reporting and field actions.Provide regulatory input during risk assessments and design control processes.QualificationsBachelor's degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field.2–5 years of experience in regulatory affairs, preferably in the medical device industry.Strong understanding of FDA regulations (21 CFR Part 820), EU MDR, and ISO 13485.Experience with regulatory submissions and product registrations in multiple global markets.Excellent written and verbal communication skills.Strong organizational and project management abilities.Preferred QualificationsRAC certification (Regulatory Affairs Certification).Experience with electronic submission systems (e.g., eSTAR, EUDAMED).Experience with MDSAP, ISO 14971 (risk management), and clinical evaluation reporting.
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