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Full Time Medical Device Engineer Jobs (NOW HIRING)

Device Engineer

Vancouver, WA · On-site

$103K - $130K/yr

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

Device Engineer

Vancouver, WA · On-site

$103K - $130K/yr

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

Provide mentorship and technical guidance to engineers working on device modeling, characterization ... Comprehensive benefits package including medical, dental, and vision insurance. * Generous Paid ...

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Medical Device Assembler - Packaging Job Type: Full-Time, Contract-to-Hire Pay & Schedule: * 1st ... Follow SOPs, work instructions, engineering drawings, and inspection procedures. * Maintain ...

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Device Engineer * Perform Development and Verification for avionics applications like flight ... US-IA-Cedar Rapids, Iowa (Collins Aerospace-IPS) Time Type: Full time Job Category: Engineering ...

Provide mentorship and technical guidance to engineers working on device modeling, characterization ... Comprehensive benefits package including medical, dental, and vision insurance. * Generous Paid ...

Device Engineer

Cedar Rapids, IA · On-site

$79K - $130K/yr

Medical, Dental, Vision Insurance * 401k, With Matching Contributions * Short-Term/Long-Term ... US-IA-Cedar Rapids, Iowa (Collins Aerospace-IPS) Time Type: Full time Job Category: Engineering ...

This job will be located full-time on site in Woburn, MA at our Headquarters and Manufacturing ... device engineering, preferably in the field of solar energy, optoelectronics, or semiconductor ...

Showing results 41-60

Full Time Medical Device Engineer information

See salary details

$21

$49

$96

How much do full time medical device engineer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for full time medical device 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 is the difference between Full Time Medical Device Engineer vs Medical Device Quality Engineer?

AspectFull Time Medical Device EngineerMedical Device Quality Engineer
Required CredentialsBachelor's in Engineering, certifications like CQA or Six Sigma beneficialBachelor's in Engineering or Life Sciences, certifications like CQE or ISO auditor
Work EnvironmentDesign labs, R&D departments, manufacturing facilitiesQuality assurance labs, compliance departments, manufacturing sites
Employer & Industry UsageMedical device companies, biotech firms, healthcare device manufacturersMedical device companies, regulatory agencies, compliance firms
Common Search & ComparisonYesYes

Full Time Medical Device Engineers focus on designing, developing, and testing medical devices, working closely with R&D teams. Medical Device Quality Engineers concentrate on ensuring products meet quality standards and regulatory requirements. Both roles are essential in the medical device industry but differ in their primary responsibilities and work environments.

More about Full Time Medical Device Engineer jobs

What cities are hiring for Full Time Medical Device Engineer jobs?

Cities with the most Full Time Medical Device Engineer job openings:

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

The most popular types of Medical Device Engineer jobs are:

What states have the most Full Time Medical Device Engineer jobs?

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

Infographic showing various Full Time Medical Device Engineer job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 96% In-person, 2% Hybrid, and 2% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Medical Device DHF Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 27 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.