MES Change Lead | Regulated Pharma Manufacturing
Listed on 2026-10-17
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Quality Assurance - QA/QC
Tailored Management in Hillsboro, OR is seeking a MES Change Specialist for a fully onsite role in a state‑of‑the‑art pharmaceutical environment. You will collaborate with manufacturing, IT, and quality teams to design, test, and maintain electronic documentation and MES changes across operations.
The ideal candidate holds a degree with 3–5 years of MES/E experience, plus hands‑on expertise with Track Wise and Veeva, and will own change management activities and CSV testing protocols.
This opportunity is for the MES Change Lead | Regulated Pharma Manufacturing role at Tailored Management.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Hillsboro, OR, United States.
This opportunity is part of our work in Management & Operations, IT & Technology.
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