1

Biomedical Product Development Engineer Jobs in Utah

Chemical Technician: I

Salt Lake City, UT ยท On-site

$14 - $16.73/hr

Conduct quality control testing to ensure consistency and efficacy of biomedical products. * Collaborate with interdisciplinary teams to optimize chemical processes in product development. Meet Your ...

Chemical Technician: I

Salt Lake City, UT ยท On-site

$14 - $16.73/hr

Conduct quality control testing to ensure consistency and efficacy of biomedical products. * Collaborate with interdisciplinary teams to optimize chemical processes in product development. Meet Your ...

Chemical Technician: I

Salt Lake City, UT ยท On-site

$16 - $19.12/hr

Conduct quality control testing to ensure consistency and efficacy of biomedical products. * Collaborate with interdisciplinary teams to optimize chemical processes in product development. Meet Your ...

next page

Showing results 1-20

Biomedical Product Development Engineer information

See Utah salary details

$36K

$80K

$120.6K

How much do biomedical product development engineer jobs pay per year?

As of Jul 6, 2026, the average yearly pay for biomedical product development engineer in Utah is $80,007.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $91,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Biomedical Product Development Engineer position, and why are they important?

To thrive as a Biomedical Product Development Engineer, you need a solid background in biomedical engineering, product design, and regulatory compliance, usually supported by a relevant engineering degree. Familiarity with CAD software, simulation tools, FDA regulations, and ISO standards is highly valuable, and some roles may require certification such as a Professional Engineer (PE) license. Excellent problem-solving skills, creativity, project management abilities, and effective communication are key soft skills that distinguish top performers in this field. These competencies ensure the successful development, testing, and delivery of safe and innovative biomedical devices that meet industry standards.

What does a Biomedical Product Development Engineer do?

A Biomedical Product Development Engineer is responsible for designing, developing, and testing medical devices and healthcare-related products. They collaborate with cross-functional teams, including scientists, regulatory specialists, and manufacturing engineers, to ensure products meet safety and regulatory standards. Their work involves prototyping, conducting validation studies, and optimizing designs for production. Additionally, they stay updated on industry advancements and compliance requirements to bring innovative solutions to market.

What are the typical challenges a Biomedical Product Development Engineer faces when bringing a new medical device to market?

Biomedical Product Development Engineers often encounter challenges such as navigating complex regulatory requirements, integrating multidisciplinary feedback, and ensuring device safety and efficacy through rigorous testing. Balancing innovative design with manufacturability and cost constraints is common, especially when working under tight deadlines. Collaboration with clinicians, quality assurance teams, and regulatory affairs professionals is an essential part of the process. Adapting quickly to feedback and addressing unforeseen technical issues are key to successfully advancing a product from concept to commercialization.

What are popular job titles related to Biomedical Product Development Engineer jobs in Utah? For Biomedical Product Development Engineer jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Biomedical Product Development Engineer jobs in Utah look for? The top searched job categories for Biomedical Product Development Engineer jobs in Utah are:

Product Development Engineer

Stark Pharma Solutions Inc

Salt Lake City, UT โ€ข On-site

Contractor

Posted 6 days ago

Be an early applicant


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:ย https://www.linkedin.com/company/99455976/