Validation Scientist

QRC Group; Aibonito (PR); On-site; USD 55,000 - 85,000; Full time

Job summary

QRC Group in Aibonito, Puerto Rico, seeks a qualified Validation Specialist to support GMP-regulated pharmaceutical processes. The role requires 1–5 years in GMP settings, experience in the pharmaceutical industry, and knowledge of aseptic/regulated processes.

You will develop and execute validation protocols, reports, and SOPs with statistical data analysis. Candidate will work on multidisciplinary projects, ensuring compliance with regulatory requirements and contributing to continuous process

Qualifications

• 1–5 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) and statistical data analysis.

Skills

GMP experience

Pharmaceutical industry knowledge

Aseptic processes

Regulatory compliance

Statistical data analysis

Multidisciplinary collaboration

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.