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Medical Device Manager Jobs in Utah (NOW HIRING)

Laborie

Medical Writer II

Salt Lake City, UT · On-site

$115K - $120K/yr

Experience working in the medical device industry preferred * Project Management experience preferred Why Laborie: Our Mission every day is to operate as a world-class specialist medical company ...

Hobbsnews

Senior Manager

Salt Lake City, UT · On-site

$140 - $200/hr

Position Summary The Senior Manager will play a pivotal role in shaping and advancing BD's materials science strategy as part of the MSSI organization, supporting the medical device sector across the ...

Ultradent Products Inc

EPMO Manager

Salt Lake City, UT · Hybrid

EPMO Manager Ultradent, a global name in oral health, is hiring an EPMO Manager to lead our project ... We're a medical device company, so getting the details right matters as much as moving fast. The ...

Ultradent Products Inc

EPMO Manager

South Jordan, UT · On-site

$100 - $130/hr

We're a medical device company, so getting the details right matters as much as moving fast. The ... What you'll doLead, coach, and grow a team of project managers -- including hiring and performance ...

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All JobsMedical Device JobsMedical Device Manager JobsMedical Device Manager Jobs in Utah

Medical Device Manager information

See Utah salary details

$10

$36

$60

How much do medical device manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical device manager in Utah is $36.12, according to ZipRecruiter salary data. Most workers in this role earn between $20.82 and $48.36 per hour, depending on experience, location, and employer.

What is a medical device manager?

Medical Device Managers are professionals responsible for overseeing the development, production, and regulatory compliance of medical devices within healthcare organizations or manufacturing companies. They coordinate teams, manage product lifecycles, ensure products meet safety standards, and liaise with regulatory bodies such as the FDA. Their work helps ensure that medical devices are safe, effective, and brought to market efficiently. In addition, they may also handle budgeting, quality assurance, and post-market surveillance of devices.

What are the key skills and qualifications needed to thrive as a medical device manager?

To excel as a Medical Device Manager, you need a solid background in biomedical engineering, regulatory compliance, and product lifecycle management, often supported by a relevant degree and industry experience. Familiarity with quality management systems (such as ISO 13485), FDA or CE regulatory processes, and CRM or ERP software is typically required. Strong leadership, problem-solving, and communication skills help in guiding cross-functional teams and managing client relationships. These competencies ensure the safe, effective launch and maintenance of medical devices in a highly regulated market.

What are some common challenges faced by medical device managers in ensuring regulatory compliance?

Medical Device Managers often encounter challenges in navigating complex and evolving regulatory requirements across different regions. Ensuring that products meet the standards set by agencies like the FDA or EMA requires continuous monitoring of changes in regulations, thorough documentation, and close collaboration with regulatory affairs and quality assurance teams. Additionally, balancing compliance with timely product development and market launch can be demanding, as even minor oversights can lead to delays or costly recalls.

What is the difference between Medical Device Manager vs Medical Equipment Coordinator?

AspectMedical Device ManagerMedical Equipment Coordinator
CertificationsRegulatory and management certifications, such as RAC or PMPBasic healthcare or equipment management certifications
Work EnvironmentHealthcare facilities, manufacturing companies, regulatory agenciesHospitals, clinics, equipment suppliers
Employer & IndustryMedical device companies, hospitals, biotech firmsHospitals, clinics, medical equipment vendors
Primary FocusOverseeing device development, compliance, and lifecycle managementManaging equipment inventory, maintenance, and distribution

The Medical Device Manager primarily focuses on overseeing the development, compliance, and lifecycle of medical devices, often requiring management certifications. In contrast, the Medical Equipment Coordinator handles equipment inventory, maintenance, and distribution within healthcare settings. Both roles are essential in healthcare but differ in scope and responsibilities.

What are the most commonly searched types of Medical Device jobs in Utah?

The most popular types of Medical Device jobs in Utah are:

What are popular job titles related to Medical Device Manager jobs in Utah?

For Medical Device Manager jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Medical Device Manager jobs in Utah look for?

The top searched job categories for Medical Device Manager jobs in Utah are:

What cities in Utah are hiring for Medical Device Manager jobs?

Cities in Utah with the most Medical Device Manager job openings:

Medical Device Manager jobs near you
Infographic showing various Medical Device Manager job openings in Utah as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $75,131 per year, or $36.1 per hour.

Medical Writer II

Laborie

Salt Lake City, UT • On-site

$115K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 16 days ago

Job description

We believe that great healthcare is an essential safeguard of human dignity.

At Laborie, we know the work we do matters - it's what fuels our motivation and contributes to our success. If you're ready to make a positive impact in the lives of patients across the globe, we'd like to meet you.

We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good.We're not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values ofAspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

Who We're Looking For:

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents for global regulatory agencies. This involves collaboration with internal and external partners to support technical, medical and clinical writing outputs for Clinical and Regulatory business needs in accordance with the relevant and evolving international standards as well as LABORIE standard operating procedures. This person will write a variety of documents for distinct audiences including Post-Market Surveillance (PMS) plans, PMS reports, Periodic Safety Update Reports (PSURs) and Proactive PMS study protocols, and will contribute to Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up Reports (PMCFERs).

About the Role:

Perform on-line external vigilance reviews and compare results to the Risk Management File.

Critically appraise, analyze, and summarize internal and external data insupport of the PMS requirements for geographies such as the EU, Health Canada, UK, etc.

Search out, review, write and maintain records of PMS data pertaining to the safety and effectiveness of Laborie devices.

Assist in ensuring all PMS requirements are met for device registrations and maintenance while working with other LABORIE team members.

Work cross functionally to develop, compile and report proactive PMS activities and integrate reporting into PMCFERs and PSURs.

Undertake various projects and tasks as assigned.

What you Bring:

  • Bachelor's degree in a scientific field or in writing/composition discipline and 5+years' experience writing PSURs. Experience with Medical Writing required.
  • Working knowledge of medical device clinical and PMS regulations, standards and guidelines (ISO, MEDDEV, MDR, IVDR, FDA CFR, UKCA, Health Canada) and experience conducting focused analysis of internal and external complaint data
  • Demonstrated ability to manage project timelines, including ability to adapt to shifting priorities and competing demands while maintaining strong attention to detail
  • Strong computer skills, proficiency with MS Office and ability to work both independently and collaboratively in a team setting
  • Excellent English verbal, written and presentation skills with great attention to detail
  • Experience working in the medical device industry preferred
  • Project Management experience preferred

Why Laborie:

Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.

  • Paid time off and paid volunteer time
  • Medical, Dental, Vision
  • Pension Plan
  • Parental Leave and Adoption Services
  • Health and Wellness Programs and Events

Laborieprovidesequal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexualorientation,or any characteristic protected underapplicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.

Employment Type: Full time

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