Senior CQV & Sterility Validation Engineer
Listed on 2026-10-11
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Engineering
Validation Engineer, Pharma Engineer
Rayze Bio, a wholly-owned subsidiary of Bristol Myers Squibb, is seeking professionals to lead CQV activities across GMP spaces and analytical systems. You will develop and execute validation strategies, environmental monitoring and sterile process validation, and support investigations and CAPA across development and manufacturing operations.
The role involves hands-on qualification of analytical equipment (HPLC/UPLC, GC, UV-Vis, TOC, particle counters) and collaboration with cross-functional
This posting is for the Senior CQV & Sterility Validation Engineer role at Bristol-Myers Squibb Co, based in Indianapolis, IN, United States.
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We are looking to fill the Senior CQV & Sterility Validation Engineer position at Bristol-Myers Squibb Co in Indianapolis, IN, United States.
The Senior CQV & Sterility Validation Engineer role at Bristol-Myers Squibb Co is now open for applications in Indianapolis, IN, United States.
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