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Biomedical Project Manager Jobs in Utah (NOW HIRING)

Adventhealth

Clinical Engineer

Murray, UT · On-site

$20.77 - $38.63/hr

... asset management. * Supports department operations through special projects, on-call coverage ... working with biomedical equipment in a clinical engineering environment [Preferred] Additional ...

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Biomedical Project Manager information

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$19

$42

$69

How much do biomedical project manager jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for biomedical project manager in Utah is $42.10, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $46.15 per hour, depending on experience, location, and employer.

What is the difference between Biomedical Project Manager vs Biomedical Engineer?

AspectBiomedical Project ManagerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biomedical Engineering, Project Management CertificationBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentProject teams, clinical settings, R&D departmentsLaboratories, manufacturing, clinical research
Employer & Industry UsageHospitals, biotech firms, medical device companiesMedical device companies, research institutions, hospitals

The Biomedical Project Manager focuses on overseeing projects, coordinating teams, and ensuring timely delivery of biomedical products. In contrast, the Biomedical Engineer is involved in designing, developing, and testing medical devices or systems. While both roles require biomedical engineering knowledge, the project manager emphasizes management skills and project execution, whereas the engineer concentrates on technical development and innovation.

What are Biomedical Project Managers?

Biomedical Project Managers are professionals responsible for overseeing and coordinating biomedical research projects, clinical trials, or product development within the healthcare or life sciences industry. They ensure that projects are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, communicating with stakeholders, and addressing potential risks or issues during the project lifecycle. Biomedical Project Managers often work closely with scientists, engineers, medical staff, and regulatory bodies to facilitate successful project outcomes.

How does a Biomedical Project Manager typically collaborate with cross-functional teams during a project lifecycle?

A Biomedical Project Manager works closely with diverse teams such as research scientists, regulatory specialists, engineers, and clinical staff to ensure project milestones are met. They facilitate communication across these groups by organizing regular meetings, tracking progress, and resolving issues that arise. This collaborative approach helps align project objectives, address challenges promptly, and maintain compliance with regulatory standards. Effective coordination and relationship-building are key to successfully delivering complex biomedical projects on time and within budget.

What are the key skills and qualifications needed to thrive as a Biomedical Project Manager, and why are they important?

To thrive as a Biomedical Project Manager, you need a solid background in biomedical sciences or engineering, project management experience, and often a relevant degree such as a BS/MS in a related field. Familiarity with project management software (e.g., MS Project, Asana), regulatory compliance systems (like FDA or ISO standards), and sometimes a PMP certification are typically important. Outstanding communication, leadership, and problem-solving skills help you coordinate cross-functional teams and manage stakeholder expectations. These competencies ensure successful project delivery, regulatory compliance, and effective collaboration in the complex biomedical industry.
What are popular job titles related to Biomedical Project Manager jobs in Utah? For Biomedical Project Manager jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Biomedical Project Manager jobs in Utah look for? The top searched job categories for Biomedical Project Manager jobs in Utah are:
What cities in Utah are hiring for Biomedical Project Manager jobs? Cities in Utah with the most Biomedical Project Manager job openings:
Biomedical Project Manager jobs near you
Infographic showing various Biomedical Project Manager job openings in Utah as of July 2026, with employment types broken down into 2% Internship, 1% As Needed, 81% Full Time, 15% Part Time, and 1% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $87,563 per year, or $42.1 per hour.

Regulatory Affairs Specialist

ELITechGroup Inc.

Logan, UT • On-site

Full-time

Re-posted 18 days ago

Job description

Summary

This role is responsible for ensuring that all products comply with applicable global regulatory requirements throughout their lifecycle-from development and registration to post-market surveillance. The Regulatory Affairs Specialist helps ensure regulatory compliance for diagnostics products with FDA, Health Canada, EU, other regulatory bodies, ISO, and business objectives.

Essential Duties and Responsibilities

  • Implement company regulatory affairs procedures.
  • Prepare, compile, and submit regulatory documentation (e.g., 510(k), PMA, CE Technical Files) to global regulatory agencies and with guidance from Regulatory Affairs Manager manage regulatory submissions.
  • Interpret and apply FDA, EU MDR, ISO 13485, and other international regulations to ensure product compliance.
  • Collaborate with cross-functional teams (R&D, Quality, Clinical, Marketing) to support product development and regulatory strategy.
  • Review and approve product labeling, instructions for use (IFUs), and promotional materials for regulatory compliance.
  • Monitor and analyze changes in regulatory requirements and communicate updates to internal stakeholders.
  • Support internal and external audits, including FDA inspections and Notified Body assessments.
  • Maintain regulatory files and databases, ensuring accurate and up-to-date documentation.
  • Participate in post-market surveillance activities, including adverse event reporting and field actions.
  • Provide regulatory input during risk assessments and design control processes.

Qualifications

  • Bachelor's degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field.
  • 2–5 years of experience in regulatory affairs, preferably in the medical device industry.
  • Strong understanding of FDA regulations (21 CFR Part 820), EU MDR, and ISO 13485.
  • Experience with regulatory submissions and product registrations in multiple global markets.
  • Excellent written and verbal communication skills.
  • Strong organizational and project management abilities.

Preferred Qualifications

  • RAC certification (Regulatory Affairs Certification).
  • Experience with electronic submission systems (e.g., eSTAR, EUDAMED).
  • Experience with MDSAP, ISO 14971 (risk management), and clinical evaluation reporting.

Job Posted by ApplicantPro