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Medical Device Processing Jobs (NOW HIRING)

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 ... Problem solving and process improvement skills. Desired Qualifications: * Experience working in ...

Gn

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... You will guide patients through the process of diagnostic testing, selection, fitting, and ...

Beltone

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... You will guide patients through the process of diagnostic testing, selection, fitting, and ...

Beltone

Medical Device Sales

Prescott, AZ · On-site

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... You will guide patients through the process of diagnostic testing, selection, fitting, and ...

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Showing results 21-40

All JobsMedical Device Processing Jobs

Medical Device Processing information

What is the difference between Medical Device Processing vs Medical Equipment Technician?

AspectMedical Device ProcessingMedical Equipment Technician
CertificationsTypically requires certification in sterilization or processingRequires certification in equipment repair or biomedical technology
Work EnvironmentCleanrooms, sterilization areas, hospitalsHospitals, clinics, repair shops
Job FocusCleaning, sterilizing, and preparing medical devicesMaintaining, repairing, and troubleshooting medical equipment
Industry UsageHospitals, medical device companies, sterilization facilitiesHospitals, biomedical service companies

Medical Device Processing primarily involves sterilizing and preparing devices for use, focusing on cleanliness and safety. Medical Equipment Technicians repair and maintain medical equipment. While both roles support healthcare, they differ in responsibilities, certifications, and work environments.

How do you become a medical device processing technician?

To become a medical device processing technician, candidates typically need a high school diploma or equivalent and may receive on-the-job training or complete a certification program in medical device processing or sterilization. Knowledge of infection control, safety protocols, and the use of sterilization equipment is essential for this role.
What cities are hiring for Medical Device Processing jobs? Cities with the most Medical Device Processing job openings:
What states have the most Medical Device Processing jobs? States with the most job openings for Medical Device Processing jobs include:
Infographic showing various Medical Device Processing job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Medical Device DHF Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 16 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