RayzeBio in Indianapolis, IN, seeks a Senior Validation Engineer, CQV Sterility Assurance to lead commissioning, qualification, and validation efforts across facility systems and analytical labs. You will partner with Quality, Manufacturing, Engineering, and QA to ensure validated state and regulatory compliance in aseptic radiopharmaceutical operations.
The role requires 4–8 years in GMP environments, strong technical writing, and hands-on CQV experience with analytical instrumentation such as
#J-18808-LjbffrSenior CQV Sterility Engineer – Validation Leader in indianapolis at Unknown Company
This position is listed as full time and onsite.