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Medical Product Development Jobs in Utah (NOW HIRING)

Mity-Lite

Director of Product Development

Orem, UT · 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 ...

Mity-Lite

Director of Product Development

Orem, UT

$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 ...

Mity-Lite

Director of Product Development

Orem, UT · 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 ...

Imh

Product Development Partner - Medicare

Murray, UT · 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 ...

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All JobsMedical Product Development JobsMedical Product Development Jobs in Utah

Medical Product Development information

See Utah salary details

$38.7K

$115.6K

$131.5K

How much do medical product development jobs pay per year?

As of Aug 10, 2026, the average yearly pay for medical 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 are the key skills and qualifications needed to thrive in medical product development?

To excel in Medical Product Development, you need a background in biomedical engineering, life sciences, or a related field, along with experience in product design and regulatory compliance. Familiarity with CAD software, quality management systems (QMS), and ISO or FDA regulatory standards is typically required. Strong project management, problem-solving abilities, and effective cross-functional communication are crucial soft skills for this role. These competencies ensure the creation of safe, innovative medical products that meet regulatory requirements and address patient needs.

What is medical product development?

Medical product development is the process of designing, creating, testing, and bringing medical devices, diagnostics, or pharmaceutical products to market. This multidisciplinary process involves stages such as research, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that products are safe, effective, and meet regulatory standards before being used by patients or healthcare professionals.

What are some common challenges faced in medical product development, and how can professionals effectively navigate them?

Professionals in Medical Product Development often encounter challenges such as navigating complex regulatory requirements, coordinating cross-functional teams, and managing tight project timelines. Success in this role requires strong project management skills, adaptability, and effective communication with stakeholders including engineers, clinicians, and regulatory experts. Building a thorough understanding of FDA or international guidelines, maintaining meticulous documentation, and fostering collaborative team environments can help overcome these obstacles and drive successful product launches.
Medical Product Development jobs near you
Infographic showing various Medical 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 Development Engineer

Stark Pharma Solutions Inc

Salt Lake City, UT • On-site

Contractor

Re-posted 11 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/