Senior CQV & Sterility Validation Engineer
Listed on 2026-10-11
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Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Biomedical Engineer
Rayze Bio in Indianapolis is seeking a Senior Validation Engineer, CQV Sterility & CQV, to draft, execute, and maintain qualification and validation documentation for GMP facilities and processes. You will collaborate with Quality, Manufacturing, Engineering, and project teams to ensure systems remain validated and compliant.
The role covers aseptic manufacturing environments, environmental monitoring, analytical equipment qualification, and validation study execution.
Are you ready to take on the Senior CQV & Sterility Validation Engineer role at Bristol Myers Squibb?
This is a strong role to take on the Senior CQV & Sterility Validation Engineer role at Bristol Myers Squibb.
As a Senior CQV & Sterility Validation Engineer, you will play an important part at Bristol Myers Squibb in Indianapolis, IN, United States.
We invite applications for the Senior CQV & Sterility Validation Engineer position located in Indianapolis, IN, United States.
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