RayzeBio in Indianapolis is seeking a Validation Engineer II, CQV Sterility Assurance to draft, execute, and maintain commissioning, qualification, and validation documentation for facility, utility, analytical, laboratory, sterility assurance, and process systems in a GMP radiopharmaceutical setting.
You will support aseptic manufacturing environments, environmental monitoring, cleanroom qualification, and GMP study execution, partnering with Quality, Manufacturing, Engineering, QC, Operations,
#J-18808-LjbffrCQV Sterility Validation Engineer II in indianapolis at Unknown Company
This position is listed as full time and onsite.