QRC Group in Aibonito, Puerto Rico is seeking a qualified Validation Specialist for GMP-regulated pharmaceutical environments. The role focuses on aseptic and regulated processes, with emphasis on developing and executing validation protocols and reports to support manufacturing quality.
You will collaborate on multidisciplinary projects, ensure regulatory compliance, and contribute to statistical data analysis to uphold product integrity and patient safety.
#J-18808-LjbffrGMP Validation Specialist – Pharma & Aseptic Expert in aibonito at Unknown Company
This position is listed as full time and onsite.