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Freelance Medical Device Design Jobs (NOW HIRING)

aspensurgical

Design Engineer

Caledonia, MI · On-site

Medical Device Product Development * Lead projects and evaluate design changes related to existing products to maintain business continuity. * Develop and evaluate medical device designs which meet ...

aspensurgical

Sr Design Engineer

Caledonia, MI

Execute medical device design history file activities to be compliant with applicable regulations * Conduct the development and evaluation of medical device designs which meet defined product ...

Aspen Surgical

Design Engineer

Caledonia, MI · On-site

Medical Device Product Development * Lead projects and evaluate design changes related to existing products to maintain business continuity. * Develop and evaluate medical device designs which meet ...

Actalent

Medical Device Engineer

Aurora, CO · Hybrid

$57.69/hr

Design, evaluate, and support electrical systems used in medical devices. * Plan, execute, and ... Support compliance efforts related to EU Medical Device Regulation (EU MDR 2017/745). * Develop ...

Aspen Surgical

Sr Design Engineer

Caledonia, MI · On-site

Execute medical device design history file activities to be compliant with applicable regulations * Conduct the development and evaluation of medical device designs which meet defined product ...

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

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Freelance Medical Device Design information

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$47

$132

How much do freelance medical device design jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for freelance medical device design in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

What is freelance medical device design?

Freelance medical device design involves independent professionals or consultants who specialize in creating, developing, and improving medical devices for clients, such as healthcare companies or startups. These freelancers may work on tasks like conceptualization, CAD modeling, prototyping, regulatory documentation, and usability testing. Their expertise helps clients navigate the complex requirements of the medical device industry, including compliance with safety and regulatory standards. By working on a freelance basis, they offer flexible, project-based support without the long-term commitment of hiring full-time staff.

What are some common challenges freelance medical device designers face when managing projects independently?

Freelance medical device designers often encounter challenges such as navigating complex regulatory requirements, managing communication with clients who may have varying levels of technical understanding, and balancing multiple projects with tight deadlines. Additionally, coordinating with external teams, such as manufacturers or clinical experts, can require strong project management and collaboration skills. Staying updated on industry standards and ensuring all design documentation is thorough are also essential to avoid costly revisions or delays.

What are the key skills and qualifications needed to thrive as a freelance medical device designer?

To thrive as a Freelance Medical Device Designer, you need a solid background in biomedical engineering or industrial design, along with knowledge of regulatory standards and prototyping. Proficiency in CAD software (like SolidWorks or AutoCAD), rapid prototyping tools, and familiarity with FDA or CE Mark certification processes is crucial. Strong problem-solving, project management, and client communication skills set top performers apart in this role. These capabilities ensure device safety, regulatory compliance, and successful collaboration with clients and manufacturers in a competitive industry.
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Freelance Medical Device Design jobs near you
Infographic showing various Freelance Medical Device Design job openings in the United States as of July 2026, with employment types broken down into 88% Full Time, 9% Part Time, and 3% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Medical Device Design Control Engineer

Prophecy Technologies

Indianapolis, IN • On-site

$123K - $148K/yr

Full-time

Posted 10 days ago

Job description

Role Overview:
This role involves supporting Design History File (DHF) activities and comprehensive risk management for medical device development projects. The engineer will be responsible for reviewing, updating, and maintaining critical documentation such as FMEAs, PHAs, Product Characterization, and Product Specifications, ensuring compliance with regulatory and quality standards throughout the product lifecycle.
Key Responsibilities:
  • Support Design History File (DHF) activities for medical device development projects.
  • Review, update, and maintain Global dFMEA documentation ensuring risks are adequately identified, analyzed, and mitigated.
  • Review, update, and maintain Global uFMEA documentation based on product use scenarios and user-related risks.
  • Develop and update Preliminary Hazard Analysis (PHA) documentation in accordance with risk management procedures.
  • Support creation and maintenance of product risk management files throughout the development lifecycle.
  • Prepare, review, and update Product Characterization documents to define product performance and design intent.
  • Create and maintain Product Specification Documents (PSD) ensuring alignment with design requirements and customer needs.
  • Develop and update Critical-to-Quality (CTQ) documents and establish measurable quality requirements.
  • Support development and maintenance of Design Input, Design Output, Verification, and Validation documentation.
  • Ensure traceability between user needs, design inputs, risk controls, verification activities, and design outputs.
  • Collaborate with Design, Quality, Regulatory, Manufacturing, and Project Management teams to support product development deliverables.
  • Participate in design reviews and provide 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 gaps in documentation 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.
  • Communicate (written and verbal) direction and project plans with appropriate personnel from other departments.

Required Skills:
  • Ability to establish document traceability between User Needs, Design Inputs, Design Outputs, Risk Management, Verification, and Validation records within Cockpit Cognition.
  • Experience 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.

Qualifications:
  • Experience: N/A

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