Biotech CQV Project Director - GMP Validation Lead

A leading engineering services company in Juncos, Puerto Rico is seeking a Project Manager for a CQV Biotech Project. The ideal candidate will lead the planning and execution of commissioning, qualification, and validation activities while ensuring compliance with cGMP standards. Responsibilities include managing CQV teams, generating progress reports, and interfacing with stakeholders. Candidates should have a Bachelor’s degree and over 8 years of experience in the biopharma sector, with at least 4 years in a leadership role. #J-18808-Ljbffr