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Medical Device Product Development Jobs in Utah (NOW HIRING)

Director of Product Development

Orem, UT ยท On-site

$145K - $155K/yr

... medical, dental, vision, life insurance, 401(k) with company match, PTO, and other employee ... product development processes, leading teams, and helping drive growth in a company that values ...

... medical, dental, vision, life insurance, 401(k) with company match, PTO, and other employee ... product development processes, leading teams, and helping drive growth in a company that values ...

Director of Product Development

Orem, UT ยท On-site

$145 - $155/hr

Director of Product Development Location: Orem, Utah. Salary: $145,000 - $155,000 per year plus ... medical, dental, vision, life insurance, 401(k) with company match, PTO, and other employee ...

Product Development Partner - Medicare

Murray, UT ยท On-site

$107K - $134K/yr

Develops new medical and ancillary products. Develops, manages, and implements strategic product ... Product development * Strategic alliances Minimum Qualifications * Ten years of experience in ...

Showing results 21-40

Medical Device Product Development information

See Utah salary details

$38.7K

$115.6K

$131.5K

How much do medical device product development jobs pay per year?

As of Aug 7, 2026, the average yearly pay for medical device product development in Utah is $115,606.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,200.00 and $130,200.00 per year, depending on experience, location, and employer.

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are popular job titles related to Medical Device Product Development jobs in Utah? For Medical Device Product Development jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Medical Device Product Development jobs in Utah look for? The top searched job categories for Medical Device Product Development jobs in Utah are:
What cities in Utah are hiring for Medical Device Product Development jobs? Cities in Utah with the most Medical Device Product Development job openings:
Infographic showing various Medical Device Product Development job openings in Utah as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $115,606 per year, or $55.6 per hour.

Product Quality Sr Designer

Zimmer, Inc.

Salt Lake City, UT โ€ข On-site

$81K - $95K/yr

Other

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet!


What You Can Expect

As a Product Quality Sr Designer, you will play a key role in refining existing documentation and ensuring continued regulatory alignment to support new and existing products.

How You'll Create Impact
  • System Design
    • Define the design approach, ensuring alignment with product objectives, user needs, clinical workflows, and system performance.
    • Translate user needs and system requirements into practical design solutions.
    • Lead to design discussions and technical reviews, evaluating alternatives and trade-offs.
    • Ensure design decisions address usability, risk mitigation, technical feasibility, and long-term product sustainability.
  • System Testing
    • Implement and review product verification and validation (V&V) testing, including developing protocols, test methods, and performance specifications.
    • Perform manual and automated testing and document results accurately.
  • Product Documentation
    • Collaborate with QA, Service, Compliance, and Regulatory teams to meet documentation requirements and ensure cross-functional alignment.
    • Create, review, and maintain risk management files, including cybersecurity risks.
    • Ensure all product requirements are documented, traceable to verifiable tests, and kept up-to-date.
    • Ensure compliance with FDA, ISO, and internal design controls.
    • Maintain the Design History File (DHF) to be complete, accurate, and regulatory-compliant, addressing gaps proactively.
What Makes You Stand Out

Strong collaboration skills across R&D, QA, clinical, and regulatory functions; able to clearly translate technical information across stakeholders.
Strong analytical skills and accurate judgment-making skills.
Ability to deal effectively with internal and external collaborators.
Excellent communications skills; written and verbal.

Your Background
  • Bachelor's degree in engineering or science related field; biomedical engineering preferred.
  • 5+ years of experience.

The ideal candidate will have a solid background in medical device design controls and product development, with direct experience in regulatory compliance and documentation.

This comes with the following:

  • Strong experience with Software as a Medical Device (SaMD).
  • Strong experience in design controls in a multi-disciplinary organization.
  • Experience drafting and maintaining DHF (design history file) content, including user needs, design inputs, design outputs, traceability matrices, and risk documentation.
  • Ability to support risk analysis (e.g. uFMEA, etc.) and contribute to usability planning and design mitigations.
  • Familiarity with ISO 14971 is required, and IEC 62366 preferred.
  • Ability to define testable requirements, support V&V protocol development, and ensure traceability in collaboration with the Product Development team.
  • Experience in a regulatory environment with strict compliance.
  • Experience with Codebeamer, Jira, or similar.
Travel Expectations

This is an in-person role in Salt Lake City, UT.

Compensation Range

$81,000 - $95,000.

Who We Are

At Orthogrid Systems, we develop advanced software applications that assist surgeons during intraoperative procedures using fluoroscopic imaging systems.

More information on our website: OrthoGrid | Zimmer Biomet


EOE/M/F/Vet/Disability

Employment Type: OTHER