CQV Validation Specialist for Biotech Downstream Equipment

A leading pharmaceutical services provider in Puerto Rico is looking for a Validation Specialist to ensure the compliance of downstream process equipment. The ideal candidate will support commissioning and qualification activities, collaborate with engineering and QA teams, and have relevant experience in GMP-regulated environments. Strong communication skills and the ability to execute validation protocols are essential for this role. Competitive candidates will also have a degree in engineering or biotechnology. #J-18808-Ljbffr