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Medical Device Support Jobs (NOW HIRING)

First Databank

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

MagVenture

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Medical Device Customer Support Technician

Alpharetta, GA · On-site

$55K - $64K/yr

We are seeking an entry-level Medical Device Customer Support Technician to serve as the first point of contact for customer service and technical support inquiries. In this role, you will handle ...

Kellton Tech

Medical Device Technician

Madison, WI · On-site

$38K - $48K/yr

Medical Device Technician Location: Madison, WI (Onsite) Scope of Work: Assemble and test medical ... support production processes. * Strong attention to detail, while multi-tasking under strict ...

TEKsystems

Mobile Device Support Specialist

Norwell, MA

$25 - $30/hr

Position Overview We are seeking a Mobile Device Support Technician to provide hands-on and remote ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

New

TEKsystems

Mobile Device Support Specialist

Norwell, MA

$25 - $30/hr

Position Overview We are seeking a Mobile Device Support Technician to provide hands-on and remote ... Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre ...

New

Equiliem

Medical Device Technician

Madison, WI · On-site

$32 - $38/hr

Medical Device Technician Madison, WI Pay: $32.00 - $38.00 per hour 26-05847 Job Summary The ... This role supports production operations through diagnostic activities, process improvement ...

ConsignMed Inc.

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Clinical Specialist Medical Device

Odessa, TX · On-site

$100 - $150/day

Provide case coverage support to Physicians, Hospital Staff, and other Healthcare Personnel to ... medical device or Operating Room experience, preferred * Gyn/Surg related experience, preferred

Gn

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... The tools and support will be provided for you to operate a first-class practice, and you will be ...

Beltone

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... The tools and support will be provided for you to operate a first-class practice, and you will be ...

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Medical Device Support information

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$29K

$45.8K

$61.5K

How much do medical device support jobs pay per year?

As of Aug 20, 2026, the average yearly pay for medical device support in the United States is $45,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $51,500.00 per year, depending on experience, location, and employer.

What is a medical device support specialist?

A Medical Device Support specialist is a professional who assists healthcare providers and patients with the installation, operation, troubleshooting, and maintenance of medical devices. They provide technical support, answer user questions, and help resolve issues related to device functionality and safety. Their role is essential in ensuring that medical equipment is used correctly and efficiently, contributing to better patient care and safety. They may also provide training and documentation to users, and sometimes liaise with manufacturers for more complex technical issues.

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

To thrive as a Medical Device Support specialist, you need a solid understanding of biomedical equipment, troubleshooting techniques, and an educational background in engineering or healthcare technology. Familiarity with device-specific software, diagnostic tools, and industry certifications like CBET (Certified Biomedical Equipment Technician) is often required. Strong problem-solving abilities, communication skills, and customer service orientation help professionals excel in assisting users and collaborating with healthcare teams. These skills ensure devices operate safely and efficiently, directly impacting patient outcomes and healthcare facility performance.

What are some typical challenges faced in a medical device support role, and how can they be addressed?

Medical Device Support professionals often encounter challenges such as troubleshooting complex technical issues, ensuring compliance with regulatory standards, and effectively communicating with both clinical staff and patients. Staying current with rapidly evolving device technologies and documentation requirements can also be demanding. These challenges can be addressed through continuous training, proactive communication, and close collaboration with engineering, quality assurance, and healthcare teams to resolve issues efficiently and maintain high standards of patient safety.
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Cities with the most Medical Device Support job openings:

What states have the most Medical Device Support jobs?

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Medical Device Support jobs near you
Infographic showing various Medical Device Support job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 22% Part Time, and 5% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $45,752 per year, or $22 per hour.

Medical Device DHF Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 24 days ago

Job description

Role Overview:
This role focuses on supporting Design History File (DHF) activities and comprehensive risk management for medical device development projects. The specialist will be responsible for reviewing, updating, and maintaining critical documentation such as dFMEA, uFMEA, and Preliminary Hazard Analysis (PHA), ensuring compliance with regulatory and quality standards throughout the product lifecycle.
Key Responsibilities:
  • Support and manage Design History File (DHF) activities for medical device projects.
  • Review, update, and maintain Global dFMEA and uFMEA documentation, identifying and mitigating risks.
  • Develop and update Preliminary Hazard Analysis (PHA) in line with risk management procedures.
  • Support the creation and maintenance of product risk management files throughout the development lifecycle.
  • Prepare, review, and update Product Characterization documents, Product Specification Documents (PSD), and Critical-to-Quality (CTQ) documents.
  • Support the development and maintenance of Design Input, Design Output, Verification, and Validation documentation.
  • Ensure robust traceability between user needs, design inputs, risk controls, verification activities, and design outputs.
  • Collaborate cross-functionally with Design, Quality, Regulatory, Manufacturing, and Project Management teams.
  • Participate in design reviews, providing technical input on risk management and DHF compliance.
  • Support engineering change assessments and associated documentation updates.
  • Review engineering documents for completeness, accuracy, and compliance with quality system requirements.
  • Identify documentation gaps and recommend corrective actions.
  • Support audits, inspections, and compliance activities related to design control and risk management documentation.
  • Contribute to continuous improvement initiatives for product development and design control processes.
  • Ensure all deliverables comply with applicable regulatory, quality, and Zimmer Biomet procedures and standards.

Required Skills:
  • Ability to establish document traceability between User Needs, Design Inputs, Design Outputs, Risk Management, Verification, and Validation records within Cockpit Cognition.
  • Experience in supporting DHF gap assessments, document linking, metadata management, and compliance reviews.
  • Familiarity with digital DHF structure, document hierarchy, and traceability matrix development.
  • Knowledge of DHF remediation projects and legacy design documentation migration into Cockpit Cognition.
  • Strong written and verbal communication skills for project plans and inter-departmental collaboration.

Qualifications:
  • Experience in medical device development environments, particularly with Design History File (DHF) and risk management processes.

Apply