CQV Validation Specialist for Biotech Downstream Equipment

A leading biotechnology services firm located in Juncos, Puerto Rico, is looking for a Validation Specialist to support the commissioning and qualification of downstream process equipment in a GMP-compliant facility. The successful candidate will have 3-7 years of CQV experience and a background in engineering or biotechnology. Key responsibilities include developing qualification protocols, ensuring compliance with regulatory standards, and interfacing with various teams. This role offers a chance to work in a collaborative environment committed to the highest ethics standards. #J-18808-Ljbffr