Validation & Engineering Group, Inc. in Puerto Rico is seeking an experienced CQV Investigation / Deviation Specialist to provide technical investigations during cleaning characterization and sterilization qualification in a GMP biologics environment.
The role involves leading or supporting deviations, reviewing manufacturing records and PI Historian data, and coordinating with Manufacturing, Quality, CQV teams to determine causes.
#J-18808-LjbffrCQV Investigation Lead: Deviation & CAPA Specialist in juncos at Unknown Company
This position is listed as full time and onsite.