CQV Validation Specialist for Biotech Downstream Equipment

A leading biotechnology services company is seeking a CQV Specialist for downstream process equipment. The role requires 3-7 years of experience in a GMP-regulated environment, focusing on developing and executing validation protocols. Key tasks include coordinating with teams, performing inspections, and ensuring compliance with regulatory standards. The ideal candidate will possess strong technical skills, including proficiency in validation systems, and excellent communication abilities. This position is located in Gurabo, Puerto Rico. #J-18808-Ljbffr