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Pharma Software Jobs in Utah (NOW HIRING)

Create and maintain a physical inventory of lab equipment, PC's, software, and any other ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

Create and maintain a physical inventory of lab equipment, PC's, software, and any other ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

Create and maintain a physical inventory of lab equipment, PC's, software, and any other ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

Pharma Software information

See Utah salary details

$71.9K

$158.4K

$187.5K

How much do pharma software jobs pay per year?

As of Jul 27, 2026, the average yearly pay for pharma software in Utah is $158,420.00, according to ZipRecruiter salary data. Most workers in this role earn between $128,800.00 and $186,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Pharma Software position, and why are they important?

To succeed in Pharma Software roles, you need strong skills in software development or engineering, a solid understanding of pharmaceutical industry regulations (such as FDA or GxP), and often a degree in computer science or a related field. Familiarity with programming languages like Python or Java, experience with validated systems, and knowledge of tools such as LIMS, ERP, or electronic lab notebooks are commonly required. Strong analytical thinking, teamwork, and effective communication set outstanding candidates apart. These abilities ensure the delivery of compliant, secure, and efficient software solutions essential for pharmaceutical operations.

What types of projects or software systems do Pharma Software professionals typically work on?

Pharma Software professionals commonly work on systems that support drug development, clinical trials, laboratory data management, and regulatory compliance, such as LIMS (Laboratory Information Management Systems), electronic data capture tools, and manufacturing execution systems. Daily tasks often include collaborating with scientists, regulatory teams, and other IT specialists to design, validate, and maintain software that must meet stringent industry regulations. This role offers unique opportunities to work at the intersection of technology and life sciences, providing valuable insights into both software engineering and pharmaceutical workflows. As you gain experience, there are career paths toward leading project teams, specializing in systems validation, or advancing into IT management within the pharmaceutical sector.

What is a Pharma Software job?

A Pharma Software job involves developing, implementing, and maintaining software solutions tailored for the pharmaceutical industry. Professionals in this role work on applications that support drug development, regulatory compliance, clinical trials, and supply chain management. They collaborate with healthcare professionals, regulatory bodies, and IT teams to ensure software meets industry standards and enhances efficiency. Skills in programming, data management, and knowledge of pharma regulations like FDA and GxP are often required.

What are popular job titles related to Pharma Software jobs in Utah? For Pharma Software jobs in Utah, the most frequently searched job titles are:
Infographic showing various Pharma Software job openings in Utah as of July 2026, with employment types broken down into 5% Locum Tenens, 2% As Needed, 88% Full Time, 2% Part Time, and 3% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $158,420 per year, or $76.2 per hour.

Product Development Engineer

Stark Pharma Solutions Inc

Salt Lake City, UT • On-site

Contractor

Posted 28 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/