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Validation Engineer — GMP & Regulatory Validation Med Devices

Job in Township of Columbia, Boone County, Missouri, USA
Listing for: Solventum
Full Time position
Listed on 2026-10-14
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Pharma Engineer, Regulatory Compliance Specialist
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 106000 - 146000 USD Yearly USD 106000.00 146000.00 YEAR
Job Description & How to Apply Below
Position: Validation Engineer — GMP & Regulatory Validation for Med Devices
Location: Township of Columbia

Solventum in Columbia, MO is seeking a Validation Engineer to ensure manufacturing processes for medical devices and drug products meet regulatory standards. You will develop and execute IQ, OQ, PQ, and PPQ protocols, and maintain comprehensive validation documentation.

You will collaborate with R&D, Manufacturing, Quality Assurance and Regulatory Affairs, provide training on validation practices, and support audits and inspections.

This role, Validation Engineer — GMP & Regulatory Validation for Med Devices at Solventum, could be your next move.

The Validation Engineer — GMP & Regulatory Validation for Med Devices role at Solventum is now open for applications in Columbia Township, MO, United States.

Join us at Solventum as our next Validation Engineer — GMP & Regulatory Validation for Med Devices in Columbia Township, MO, United States.

We are currently recruiting a Validation Engineer — GMP & Regulatory Validation for Med Devices for our team in Columbia Township, MO, United States.

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