Senior Validation Engineer - GMP/MES Specialist
Listed on 2026-10-07
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Engineering
Validation Engineer, Pharma Engineer, Quality Engineering
Syner-G seeks a Sr. Validation Engineer with 7–11 years of experience to lead validation activities across equipment, utilities, facilities, computerized systems, MES/e platforms within GMP environments.
You will develop, execute, review, and manage validation lifecycle documentation ensuring regulatory expectations and data integrity. The role partners with Manufacturing, Quality, Validation, Automation, and IT/OT teams to ensure successful deployment, qualification, and ongoing compliance.
This posting is for the Senior Validation Engineer - GMP/MES Specialist role at Syner G, based in Greenville, NC, United States.
Consider building your career as a Senior Validation Engineer - GMP/MES Specialist at Syner G.
The Senior Validation Engineer - GMP/MES Specialist position in the Bio & Pharmacology & Health, Engineering field is open for applications.
We have an opening for a Senior Validation Engineer - GMP/MES Specialist in Greenville, NC, United States within Bio & Pharmacology & Health, Engineering.
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