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Medical Device Rf Engineering Jobs (NOW HIRING)

... Engineering, LifeSciences (Pharmaceutical, Scientific, Medical Device, Diagnostics, Biotech ... RF Engineer will be a key part of the Engineering development team, developing innovative analog ...

RF Engineering Tech

Tempe, AZ · On-site

$26.68 - $40.14/hr

What you'll do We are looking for an RF Engineering Test Tech to join out team! You will work in a ... medical, financial, and/or other benefits, dependent on the position offered. Learn more about ...

... Engineering, LifeSciences (Pharmaceutical, Scientific, Medical Device, Diagnostics, Biotech ... RF Engineer will be a key part of the Engineering development team, developing innovative analog ...

... device manufacturers worldwide. Innovations from Mattson Technology in Atomic Surface Engineering ... Job Summary The RF Engineer I is an entry-level engineering professional responsible for supporting ...

You will be working alongside the Electrical and RF Engineering teams to interface with Avionics ... Design device simulators deployed across component subsystem and HITL testbeds * Collaborate with a ...

General Manager Requirements Process Engineering & Manufacturing Leadership * Own process ... Experience leading technical work or teams in aerospace, defense, medical device, RF/microwave, or ...

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Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

RF Engineer

Aberdeen Proving Ground, MD · On-site

$86K - $138K/yr

Interest in reverse engineering or RF device teardown work Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending ...

RF Engineer

Aberdeen Proving Ground, MD · On-site

$86K - $138K/yr

Interest in reverse engineering or RF device teardown work Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending ...

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Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

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Follow SOPs, work instructions, engineering drawings, and inspection procedures. * Maintain ... Medical device manufacturing experience preferred; 2+ years is highly desirable. * Experience in an ...

... device manufacturers worldwide. Innovations from Mattson Technology in Atomic Surface Engineering ... Job Summary The RF Engineer I is an entry-level engineering professional responsible for supporting ...

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Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

Showing results 41-60

Medical Device Rf Engineering information

See salary details

$37K

$117.7K

$183K

How much do medical device rf engineering jobs pay per year?

As of Sep 10, 2026, the average yearly pay for medical device rf engineering in the United States is $117,680.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $139,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Medical Device Rf Engineering jobs?

For Medical Device Rf Engineering jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Rf Engineering job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $117,680 per year, or $56.6 per hour.

Medical Device DHF Engineer

Indianapolis, IN • On-site

Prophecy Technologies
Professional, Scientific, and Technical Services • 11 - 50 employees

Full-time

Re-posted 15 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.