Validation Specialist

Aibonito, Puerto Rico | Posted on 08/04/2026

We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes.

Requirements

• 3 to 5 years of experience in a GMP environment.
  
• Experience in the pharmaceutical industry.
  
• Knowledge of and experience with aseptic and regulated processes.
  
• Experience developing and executing:
  • Validation protocols.
    
  • Validation reports.
    
  • SOPs (Standard Operating Procedures).
    
  • Statistical data analysis.
    
• Ability to work on multidisciplinary projects and comply with regulatory requirements.