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Verification Engineer

Job in Madison, Dane County, Wisconsin, 53774, USA
Listing for: Medasource
Contract position
Listed on 2026-07-13
Job specializations:
  • Engineering
    Biomedical Engineer, Medical Device Industry, Quality Engineering, Test Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 90000 USD Yearly USD 60000.00 90000.00 YEAR
Job Description & How to Apply Below

Duration: 6 Month Contract - potential for extensions

Start Date: ASAP

About the Opportunity

Our client is seeking multiple Verification Engineers to support a leading medical device team during a critical phase of product development. This role will focus on verification testing for an existing microwave ablation platform and new product enhancements, helping ensure devices meet engineering requirements prior to release.

This is an excellent opportunity for early to mid career engineers who enjoy hands on laboratory work, detailed documentation, and working in a regulated medical device environment.

Responsibilities
  • Execute verification protocols for medical device hardware and software
  • Perform hands on testing of medical devices according to established engineering procedures
  • Record, analyze, and document test results with a high level of accuracy
  • Identify failures or unexpected results and communicate findings to the engineering team
  • Complete verification reports and maintain detailed engineering documentation
  • Support software verification by executing predefined test cases and documenting pass/fail results
  • Participate in verification testing involving animal tissue (cow liver) to evaluate device performance
  • Collaborate with cross functional engineering teams to support product development and design changes
Preferred Qualifications
  • Bachelor's degree in Engineering or a related technical discipline
  • Experience executing verification or validation protocols within a regulated industry
  • Strong documentation and technical writing skills
  • Hands on laboratory or product testing experience
  • Detail oriented with excellent organizational skills
  • Ability to work independently while collaborating effectively with engineering teams
  • Strong verbal and written communication skills
Nice to Have
  • Medical device industry experience
  • Technical writing experience, including user manuals or Instructions for Use (IFUs)
  • Experience with Quality Management Systems (QMS), Product Lifecycle Management (PLM), or other engineering documentation systems
  • This role is primarily onsite in Madison, WI, as most verification testing is performed in the laboratory. Some documentation activities may be completed remotely.
  • Candidates should be comfortable working in a laboratory environment that includes testing on animal tissue (cow liver). No live animal testing is involved.
Why This Opportunity?
  • Join an innovative medical device engineering team during an exciting period of product development
  • Gain hands on experience supporting products that directly impact patient care
  • Work alongside experienced R&D and Verification Engineers
  • Excellent opportunity for engineers looking to grow their verification and validation experience within the medical device industry
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