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Medical Device Cybersecurity Jobs in Utah (NOW HIRING)

... medical device software, including software incorporating artificial intelligence, for new and ... cybersecurity considerations, and implementation of software changes throughout the product ...

... Medical Record (EMR) assistance. This role troubleshoots hardware, peripherals, and basic EMR ... Device Deployment & Lifecycle: Install, configure, relocate, and retire endpoint hardware. Prepare ...

IT Intern

Salt Lake City, UT · On-site

$14.50 - $19.25/hr

... device provisioning • Monitor and troubleshoot system issues, including analysis of security ... Pursuing a Bachelor's or Master's degree in Information Systems, Computer Science, Cyber Security, ...

Medical Device Cybersecurity information

What are some common challenges faced by professionals in medical device cybersecurity, and how can they be addressed?

Professionals in medical device cybersecurity often encounter challenges such as integrating security measures into legacy devices, ensuring compliance with evolving regulations, and balancing usability with robust protection. Collaborative efforts with engineering, regulatory, and clinical teams are crucial to embedding security throughout the product lifecycle. Staying current with threat intelligence and participating in cross-functional risk assessments also help anticipate and address vulnerabilities proactively.

What is medical device cybersecurity?

Medical device cybersecurity refers to the protection of medical devices and the data they process from cyber threats and unauthorized access. As medical devices become increasingly connected to hospital networks and the internet, robust cybersecurity measures are essential to ensure patient safety and protect sensitive health information. This field involves identifying vulnerabilities, implementing safeguards, and complying with regulatory requirements to reduce the risk of cyberattacks on medical technology.

What is the difference between Medical Device Cybersecurity vs Medical Device Quality Assurance?

AspectMedical Device CybersecurityMedical Device Quality Assurance
Required CredentialsCertifications in cybersecurity, such as CISSP or CISA; knowledge of medical device regulationsCertifications in quality management, like CQE or ISO 13485 auditor
Work EnvironmentIT security teams, R&D, regulatory compliance in healthcare settingsManufacturing, clinical, and regulatory environments focused on product quality
Employer & Industry UsageMedical device manufacturers, healthcare providers, cybersecurity firmsMedical device companies, regulatory agencies, quality assurance firms

Medical Device Cybersecurity focuses on protecting medical devices from cyber threats, ensuring data integrity and security. Medical Device Quality Assurance emphasizes maintaining product quality, safety, and compliance throughout development and manufacturing. While both roles support patient safety, cybersecurity specialists address digital vulnerabilities, whereas quality assurance professionals ensure the device meets regulatory standards.

What are the key skills and qualifications needed to thrive in medical device cybersecurity, and why are they important?

To thrive in Medical Device Cybersecurity, you need a solid background in cybersecurity principles, risk management, and biomedical engineering, often supported by a relevant degree and certifications like CISSP or CISM. Familiarity with regulatory standards (such as FDA cybersecurity guidelines), network security tools, and vulnerability assessment systems is essential. Strong analytical thinking, attention to detail, and effective communication skills help professionals collaborate with cross-functional teams and address complex security challenges. These skills are crucial to ensure medical devices remain secure from cyber threats, protecting patient safety and maintaining regulatory compliance.

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

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

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

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

Infographic showing various Medical Device Cybersecurity 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.

Principal Quality Engineer

Zimmer, Inc.

Salt Lake City, UT • On-site

Full-time

Re-posted 11 days ago


Job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.


What You Can Expect

The Principal Software Quality Engineer supports the design, development, and lifecycle support of medical device software, including software incorporating artificial intelligence, for new and existing products. This role works closely with design and cross-functional teams to support new product introductions, maintain software design documentation, and ensure compliance with applicable quality, regulatory, and industry standards. The position plays a key role in risk management, verification and validation activities, design reviews, cybersecurity considerations, and implementation of software changes throughout the product lifecycle.

How You'll Create Impact
  • Partner with design and cross-functional development teams to support software activities for new product introductions.
  • Lead or contribute to software architecture, design, implementation, integration, and maintenance for product development projects.
  • Maintain software design documentation and ensure it remains current throughout the product lifecycle.
  • Support software changes, enhancements, defect corrections, and sustaining engineering activities for released products.
  • Lead software risk management activities, including hazard analysis, risk assessments, and implementation of risk controls.
  • Support verification and validation planning, protocol development, execution, and documentation.
  • Participate in design reviews and provide technical guidance to ensure robust, compliant, and maintainable software solutions.
  • Collaborate with quality, regulatory, systems, and test engineering teams to support compliance with internal procedures and external standards.
  • Review and approve technical documentation, including software requirements, architecture and design documents, test protocols, traceability matrices, and change records.
  • Ensure software development activities align with design controls, software development lifecycle processes, and applicable regulatory expectations.
  • Provide technical leadership for complex troubleshooting, root cause investigations, and continuous improvement initiatives.
  • Mentor engineers and serve as a technical leader across multiple projects and product platforms.
  • Support audit, inspection, and regulatory submission readiness activities as needed.
What Makes You Stand Out
  • Familiarity with AAMI TIR97.
  • Knowledge of medical device cybersecurity principles and applicable standards, including ANSI/AAMI/UL 81001-5-1.
  • Experience supporting cybersecurity-by-design activities for connected or software-enabled medical devices.
Your Background
  • Bachelor's degree in Software Engineering, Computer Science, Electrical Engineering, or related technical field; advanced degree preferred.
  • 5+ years experience in software engineering, including technical leadership for complex product development programs.
  • Strong knowledge of IEC 62304 software development lifecycle processes, software design, and change management.
  • Familiarity with FDA software-related guidances and expectations.
  • Experience working within a quality management system compliant with ISO 13485.
  • Understanding of artificial intelligence applications in medical devices, including associated development and regulatory considerations.
  • Strong written and verbal communication skills.
  • Proven ability to work effectively across cross-functional teams and influence technicaldecisions.
Physical Requirements
Travel Expectations

Up to 15%

Salary Expectations:

$115,000-$140,000k based on experience


EOE/M/F/Vet/Disability

Employment Type: OTHER