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Medical Device Service Engineer Jobs (NOW HIRING)

Collabera

Medical device engineer

North Chicago, IL

... services and solutions companies globally. As a half a billion dollar IT company, Collabera ... Evaluate and integrate relevant engineering advances for improving or solving problems Understand ...

BEPC INC

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

All Companies

Field Service Engineer

Charleston, WV · On-site

Field Service Engineer Department: Service Reporting to: Regional Service Manager Location: Travel ... independent medical device service provider specializing in multi-vendor service and asset ...

BEPC INC

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

BEPC INC

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

BEPC INC

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

Orion Talent

Field Service Engineer I

Columbus, GA · On-site

$27/hr

Description The Field Service Engineer - Medical Equipment is responsible for installing ... Biomedical equipment or medical device service experience. * Healthcare technology experience.

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$22 - $24/hr

Pay Rate Low: 22 | Pay Rate High: 24 A medical device manufacturer is seeking a Production/Assembly ... Collaborate with supervisors, engineers, and technicians to resolve line issues and suggest ...

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Medical Device Service Engineer information

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$21

$49

$96

How much do medical device service engineer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for medical device service engineer in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What cities are hiring for Medical Device Service Engineer jobs?

Cities with the most Medical Device Service Engineer job openings:

What states have the most Medical Device Service Engineer jobs?

States with the most job openings for Medical Device Service Engineer jobs include:

What are popular job titles related to Medical Device Service Engineer jobs?

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Infographic showing various Medical Device Service Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, and 3% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Medical Device DHF Engineer

Indianapolis, IN • On-site

Prophecy Technologies
Professional, Scientific, and Technical Services • 11 - 50 employees
Learn more about Prophecy Technologiesexternal

Full-time

Re-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