RayzeBio, 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
#J-18808-LjbffrSenior CQV & Sterility Validation Engineer in indianapolis at Unknown Company
This position is listed as full time and onsite.