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Contract Medical Device Design Jobs (NOW HIRING)

VOLT

Medical Device Assembler

Plymouth, MN · On-site

$17.50 - $18.75/hr

... contract opportunity. Schedule: 1st Shift : 5:00 AM - 3:30 PM Monday through Thursday The ideal ... Experience as a Medical Device Assembler or Production Assembler. * Strong attention to detail ...

ICU Medical

Senior Engineer, R&D

Salt Lake City, UT

$101.10K - $138.90K/yr

The ideal candidate will bring extensive hands-on experience in medical device design and development, with a strong background in documentation, testing, and risk management. Essential Duties ...

ICU Medical

Senior Engineer, R&D

Salt Lake City, UT · On-site

$101.10K - $138.90K/yr

The ideal candidate will bring extensive hands-on experience in medical device design and development, with a strong background in documentation, testing, and risk management. Essential Duties ...

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

As of May 30, 2026, the average hourly pay for contract medical device design 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 Contract Medical Device Design vs Medical Device Design Engineer?

AspectContract Medical Device DesignMedical Device Design Engineer
CredentialsTypically requires a degree in engineering or related field; certifications like ISO 13485 are a plusRequires a degree in biomedical, mechanical, or electrical engineering; professional certifications may enhance prospects
Work EnvironmentProject-based, often freelance or consulting; varies by client and project scopeFull-time employment within a company or R&D department
Employer & Industry UsageUsed by consulting firms, contract agencies, and medical device startupsEmployed by medical device companies, hospitals, or research institutions

Contract Medical Device Design professionals focus on project-specific work, often freelance, while Medical Device Design Engineers are typically employed full-time within organizations. Both roles require similar technical credentials but differ in work setting and employment structure.

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Contract Medical Device Design jobs near you

Test Engineer - Verification & Validation - medical device

InnoTech Staffing

Manchester, NH • On-site

Full-time

Posted yesterday

Job description

InnoTECH Staffing has an immediate opening for a Test Engineer to work in a dynamic medical device R&D environment at our client who is located in Manchester, NH.

This requires being onsite 5 days a week and must be a US Citizen or Greencard holder.

Test Engineering is a high-visibility role with a significant, direct impact on the success of the project.
How you will make an impact as a Verification and Validation Test Engineer:

  • Developing and writing test procedures assessing end-to-end performance and reliability of user interfaces and hardware
  • Understanding device design and core technologies in order to inform test method development
  • Determining test coverage for revisions to design
  • Creating and evaluating test fixtures if needed for product design verification
  • Contributing to design failure investigations that may impact Risk Assessments, Hazard Analyses, and FMEAs
  • Contributing toward regulatory and agency submissions
  • Authoring Test Summaries and other documents

To be successful in this role as a Verification and Validation Test Engineer, you will need the following skills and experience:

  • Must have a BS in Physics, Biology, Electrical, Mechanical, or Biomedical Engineering.
  • Experience with research, development, and product testing
  • Experience writing procedures for others to follow
  • Experience with data and failure analysis
  • Broad measurement instrument knowledge
  • Knowledge and deep understanding of engineering fundamentals
  • Demonstrated problem solving ability and techniques
  • Ability to work as part of an interdisciplinary team
  • Self-motivated and able to self-prioritize
  • Ability to clearly explain objectives
  • Must be detail oriented and have excellent verbal and written communication skills
  • Experience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred