GMP Documentation & Compliance Specialist

A pharmaceutical company located in Barceloneta, Puerto Rico is seeking a Documentation Compliance Specialist to ensure compliance with documentation processes and standards. This role involves managing documentation workflows, supporting regulatory inspections, and maintaining comprehensive quality assurance practices. Candidates should possess a Bachelor's degree in a relevant field and have at least two years of experience in the pharmaceutical industry. Strong skills in MS Office and knowledge of manufacturing practices are essential. #J-18808-Ljbffr