RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is seeking a Validation Engineer II, CQV Sterility Assurance in Indianapolis to support GMP commissioning, qualification, and validation activities for facility and process systems. You will partner with Quality, Manufacturing, Engineering, QC, and Operations to maintain validated state and regulatory alignment.
The role covers aseptic processing, environmental monitoring, analytical equipment qualification, and lifecycle validation.
#J-18808-LjbffrCQV & Sterility Validation Engineer II in indianapolis at Unknown Company
This position is listed as full time and onsite.