Validation Engineer: GMP, MES & CSV Specialist
Listed on 2026-10-02
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Engineering
Quality Engineering, Pharma Engineer -
Quality Assurance - QA/QC
Quality Engineering
Syner-G is seeking a Validation Engineer with 4–7 years of experience to support validation across equipment, utilities, facilities, computerized systems, and MES/e platforms in GMP environments. You will develop, execute, review, and maintain validation docs ensuring data integrity and regulatory alignment.
The role involves MES/e implementation support, cross-functional collaboration, and system release activities to ensure quality and compliance in manufacturing processes.
We have an opening for a Validation Engineer: GMP, MES & CSV Specialist in United States within Engineering.
This role, Validation Engineer: GMP, MES & CSV Specialist at Syner G, could be your next move.
Are you ready to take on the Validation Engineer: GMP, MES & CSV Specialist role at Syner G?
We would love to welcome a new Validation Engineer: GMP, MES & CSV Specialist to our group in United States.
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