Validation Specialist

QRC Group; Aibonito (PR); On-site; USD 65,000 - 85,000; Full time

Job summary

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.

Qualifications

• 3–5 years of experience in a GMP environment.
• Experience in the pharmaceutical industry.
• Knowledge of aseptic and regulated processes.
• Experience developing and executing validation protocols.
• Experience developing validation reports and SOPs.
• Experience performing statistical data analysis.

Responsibilities

• Develop and execute validation protocols and reports for GMP environments.
• Create and maintain SOPs and ensure regulatory compliance.
• Collaborate on multidisciplinary projects to meet quality standards.
• Perform statistical data analysis to support process validation.

Skills

GMP experience

Pharmaceutical industry experience

Aseptic processes

Regulated processes

Statistical data analysis

Job description

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.