Jr. Validation Specialist

QRC Group; Aibonito (PR); On-site; USD 42,000 - 62,000; Full time

Job summary

QRC Group in Aibonito, Puerto Rico is seeking a Jr. Validation Specialist to support aseptic and regulated processes. The role involves developing and executing validation protocols, compiling validation reports, and maintaining SOPs to meet GMP standards.

The candidate should hold a Bachelor in Sciences with at least 2 years of GMP experience and be able to work on multidisciplinary projects while ensuring compliance with regulatory requirements, data analysis, and documentation accuracy.

Qualifications

• Bachelor degree in sciences with 2 years GMP experience.
• Experience with aseptic and regulated processes.
• Develop and execute validation protocols, validation reports, and SOPs.
• Ability to work on multidisciplinary projects and comply with regulatory requirements.

Responsibilities

• Develop and execute validation protocols.
• Develop and execute validation reports.
• Develop and execute SOPs.
• Analyze statistical data.

Skills

GMP experience

Aseptic processes

Regulatory compliance

Cross-disciplinary teamwork

Education

Bachelor in Sciences

Job description

Aibonito, Puerto Rico | Posted on 11/05/2026

We are looking for a qualified Jr. Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing:

• Validation protocols.
  
• Validation reports.
  
• SOPs (Standard Operating Procedures).
  
• Statistical data analysis
  

Requirements

• Bachelor in Sciences with 2 years of experience in a GMP environment preferably in the pharmaceutical industry
  
• Ability to work on multidisciplinary projects and comply with regulatory requirements.
  
• Experience with aseptic and regulated processes and developing and executing: Validation protocols, Validation reports, and SOPs (Standard Operating Procedures).