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Manager Medical Device Software Engineer Jobs in Utah

Danaher

Software Engineer Internships

Ogden, UT · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Ogden, UT

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Orem, UT · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Logan, UT

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Orem, UT

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

West Jordan, UT · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Logan, UT · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Gehc

Sr Software Engineer

Salt Lake City, UT · On-site

$118K - $156K/yr

Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management ... Medical device development * Aerospace or defense systems * Automotive systems * Industrial ...

GE HealthCare

Sr Software Engineer

Salt Lake City, UT · On-site

$117K - $154K/yr

Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management ... Medical device development * Aerospace or defense systems * Automotive systems * Industrial ...

Motorola

Software Engineer

Salt Lake City, UT · Remote

Cloud systems used to manage distributed edge appliances in the field Technical leadership ... Design systems for remote device provisioning, configuration, and software updates * Improve ...

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All JobsManager Medical Device Software Engineer JobsManager Medical Device Software Engineer Jobs in Utah

Manager Medical Device Software Engineer information

What are the key skills and qualifications needed to thrive as a Manager Medical Device Software Engineer, and why are they important?

To thrive as a Manager Medical Device Software Engineer, you need expertise in software development, medical device regulations (such as FDA or ISO 13485), and a background in engineering or computer science, often supported by advanced degrees or certifications. Familiarity with tools like version control systems (e.g., Git), embedded systems platforms, and quality management software is essential, along with understanding regulatory documentation processes. Strong leadership, effective communication, and problem-solving abilities distinguish top performers in this role. These skills are crucial for ensuring safe, compliant, and innovative medical device software development while leading teams to deliver high-quality products.

How does a Manager Medical Device Software Engineer typically collaborate with cross-functional teams during product development?

A Manager Medical Device Software Engineer frequently works alongside teams such as regulatory affairs, quality assurance, hardware engineering, clinical specialists, and marketing. They coordinate software development activities to ensure compliance with industry standards and regulatory requirements, while also aligning software features with clinical and business needs. These managers often lead design reviews, facilitate risk assessments, and ensure effective communication between software engineers and non-technical stakeholders. This collaborative environment is essential for delivering safe, effective, and user-friendly medical devices.

What does a Manager Medical Device Software Engineer do?

A Manager Medical Device Software Engineer oversees teams that design, develop, and maintain software for medical devices. They ensure that the software complies with regulatory standards, works reliably, and meets the needs of healthcare professionals and patients. In addition to technical leadership, they coordinate with cross-functional teams, manage project timelines, and mentor engineers. Their role is critical in ensuring products are both safe and effective for use in medical settings.
What are the most commonly searched types of Medical Device Software Engineer jobs in Utah? The most popular types of Medical Device Software Engineer jobs in Utah are:
What are popular job titles related to Manager Medical Device Software Engineer jobs in Utah? For Manager Medical Device Software Engineer jobs in Utah, the most frequently searched job titles are:
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What cities in Utah are hiring for Manager Medical Device Software Engineer jobs? Cities in Utah with the most Manager Medical Device Software Engineer job openings:
Manager Medical Device Software Engineer jobs near you

Principal Quality Engineer

Zimmer, Inc.

Salt Lake City, UT • On-site

Other

Posted 3 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

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