Senior Validation Engineer - GMP Process Automation
Listed on 2026-10-07
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Engineering
Validation Engineer, Pharma Engineer
Bristol Myers Squibb seeks a Senior Validation Engineer to qualify process control and MES systems in a GMP biologics facility. You will oversee protocol generation, execution, issue resolution, and approval of qualification activities to ensure readiness for use and regulatory compliance.
The role involves coordinating validation for DeltaV and Syncade, supporting operations, and leading technical writing and project management efforts in a highly automated environment.
The following opportunity is for a Senior Validation Engineer - GMP Process Automation with Bristol-Myers Squibb.
Join us at Bristol-Myers Squibb as our next Senior Validation Engineer - GMP Process Automation in Harvard, MA, United States.
We are currently recruiting a Senior Validation Engineer - GMP Process Automation for our team in Harvard, MA, United States.
This is an excellent opportunity to take on the Senior Validation Engineer - GMP Process Automation role at Bristol-Myers Squibb.
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