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Validation Engineer

Job in Jacksonville, Duval County, Florida, 32290, USA
Listing for: Insight Global
Full Time position
Listed on 2025-12-23
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 25 - 35 USD Hourly USD 25.00 35.00 HOUR
Job Description & How to Apply Below

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This range is provided by Insight Global. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$25.00/hr - $35.00/hr

Job Description

One of our large medical device companies is seeking a Validation Engineer to join their team. The Validation Engineer will be a key contributor to validating a very high visibility raw material implementation project at the site. They will successfully lead and support the following activities with their cross-functional and Engineering team partners:

  • Plans, conducts and manages multiple engineering and material implementation/validation projects across various manufacturing platforms.
  • Develops, implements and qualifies material, equipment and/or process enhancements/changes that will aid in qualification of the highest priority material implementation
  • Strong analytical approach to problem solving to deliver innovative solutions.
  • Project Management to qualify materials, processes, equipment, systems and/or equipment
  • Root cause analysis for problem solving and improvement of manufacturing equipment, processes, and systems.
  • Responsible for all associated project documentation to include those that involve change management and quality system.
  • Work with agility to solve unplanned downtime or excessive rejects during protocols to develop solutions to successfully complete validations and testing.
  • Performs justification of capital and expense projects for project development of a medium complexity. This position pays $25-30/hour depending on experience.
Required Skills and Experience
  • Experience with working in submitting test documentation and managing change requests.
  • Experience working with nonconformance investigations and CAPAs
  • Experience working in a regulated industry environment
Nice to Have Skills and Experience
  • Experience working with validations and processing technical documents (DOE/IQ/OQ/PQ)
  • Medical Devices industry experience
  • Achievement of Six Sigma/Green Belt/Black Belt accreditation is a plus.
Seniority level
  • Associate
Employment type
  • Contract
Job function
  • Medical Equipment Manufacturing

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Inferred from the description for this job
  • Medical insurance
  • 401(k)
  • Vision insurance
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