Validation Scientist

QRC Group, LLC; Aibonito (PR); On-site; USD 60,000 - 85,000; Full time

Job summary

QRC Group, LLC in Aibonito, Puerto Rico is seeking a qualified Validation Specialist to support GMP-regulated pharmaceutical processes. The role focuses on validating protocols, reports, and SOPs while ensuring compliance with regulatory requirements.

The candidate will contribute to multidisciplinary projects, perform statistical data analysis, and work in a regulated environment with emphasis on aseptic techniques.

Qualifications

• 1 to 5 years of GMP experience.
• 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.

Skills

GMP experience

Pharma industry

Aseptic processes

Validation protocols

Validation reports

SOPs

Stats analysis

Regulatory compliance

Cross-functional teamwork

Job description

Aibonito, Puerto Rico | Posted on 07/27/2026

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

Requirements

• 1 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.