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Medical Device Product Development Jobs in Utah (NOW HIRING)

A-Line Staffing Solutions

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Assembler - Medical Devices

Sandy, UT · On-site

$25/hr

... and product characterization activities. The position plays a critical role in the development and fabrication of medical device components while ensuring adherence to quality standards ...

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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 28, 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:

Medical Device Product Development jobs near you
Infographic showing various Medical Device Product Development job openings in Utah as of August 2026, with employment types broken down into 79% Full Time, 17% Part Time, and 4% Contract. Highlights an 90% In-person, 4% Hybrid, and 6% Remote job distribution, with an average salary of $115,606 per year, or $55.6 per hour.

Product Development Engineer

Stark Pharma Solutions Inc

Salt Lake City, UT • On-site

Contractor

Re-posted 29 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Product Development Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity.

Job Title: Product Development Engineer
Location: Salt Lake City, UT
Duration: Long Term

Position Overview

We are seeking an experienced Product Development Engineer to support the development of a Software as a Medical Device (SaMD) within a regulated medical device environment. This role focuses on developing and maintaining Design History File (DHF) documentation, defining system and product requirements, supporting risk management and verification activities, and ensuring compliance with FDA Quality Management System (QMS) requirements and applicable medical device standards throughout the product development lifecycle.

Key Responsibilities

  • Develop and maintain Design History File (DHF) documentation, including user needs, design inputs, system requirements, traceability matrices, and risk management files.
  • Define clear, complete, and testable system requirements while maintaining end-to-end traceability.
  • Support risk management activities, including FMEA and risk documentation in accordance with ISO 14971.
  • Participate in Verification & Validation (V&V) activities by developing test protocols, executing test cases, and documenting results.
  • Collaborate with Engineering, Quality Assurance, Clinical, and Regulatory teams to support product development activities.
  • Ensure compliance with FDA Quality Management System (QMS) requirements and applicable regulatory standards.
  • Support usability engineering activities following IEC 62366 guidelines.
  • Utilize Codebeamer, JIRA, or similar requirements management and traceability tools.
  • Contribute to continuous improvement initiatives throughout the product development lifecycle.

Required Qualifications

  • Bachelor's degree in Engineering or a related scientific discipline (Biomedical Engineering preferred).
  • 5+ years of experience in Product Development, Systems Design, or related engineering roles within a regulated environment.
  • Hands-on experience supporting Software as a Medical Device (SaMD) development.
  • Strong experience creating and maintaining Design History File (DHF) documentation, including user needs, requirements, traceability matrices, and risk files.
  • Working knowledge of ISO 14971; familiarity with ISO 62304 and IEC 62366.
  • Experience working within FDA Quality Management System (QMS) requirements.
  • Experience using Codebeamer, JIRA, or similar requirements management and traceability tools.
  • Experience supporting Verification & Validation (V&V) activities.
  • Strong analytical, technical, documentation, written, and verbal communication skills.
  • Ability to collaborate effectively with multidisciplinary and cross-functional teams.

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 your best contact number and the best time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/