Validation Engineer/Molding

QRC Group, LLC; Aibonito (PR); On-site; USD 60,000 - 80,000; Full time

Job summary

QRC Group, LLC in Aibonito, Puerto Rico seeks a Validation Specialist to support validation activities within the Injection Molding area. The candidate will assist in executing, documenting, and completing validation projects while ensuring compliance with quality standards and regulatory requirements.

You will collaborate with Manufacturing, Engineering, Quality, and Validation teams to meet project objectives and maintain rigorous cGMP-compliant documentation.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical field.
• Previous experience in validation activities within a regulated environment (Medical Device, Pharmaceutical, or Manufacturing) preferred.

Responsibilities

• Support the execution of validation protocols for molding processes and equipment.
• Collect, analyze, and document validation data and results.
• Collaborate with Manufacturing, Engineering, Quality, and Validation teams to ensure project objectives are met.
• Assist in investigation and resolution of validation-related issues, deviations, and corrective actions.
• Maintain accurate documentation in compliance with cGMP requirements and internal procedures.
• Participate in continuous improvement initiatives and provide technical support as needed.
• Ensure assigned activities are completed within established timelines and quality standards.

Skills

Validation

Documentation

Collaboration

Problem solving

Education

Bachelor's degree

Job description

Aibonito, Puerto Rico | Posted on 08/25/2026

We are seeking a Validation Specialist tosupport validation activities within the Injection Molding area. The selected candidatewill assist in the execution, documentation, and completion of validationprojects while ensuring compliance with quality standards and applicableregulatory requirements.

Key Responsibilities

• Support the execution ofvalidation protocols for Molding processes and equipment.
  
• Collect, analyze, and documentvalidation data and results.
  
• Collaborate with Manufacturing,Engineering, Quality, and Validation teams to ensure project objectivesare met.
  
• Assist in the investigation andresolution of validation-related issues, deviations, and correctiveactions.
  
• Maintain accurate documentationin compliance with cGMP requirements and internal procedures.
  
• Participate in continuousimprovement initiatives and provide technical support as needed.
  
• Ensure assigned activities arecompleted within established timelines and quality standards.
  

Requirements

• Bachelor’s degree inEngineering, Life Sciences, or a related technical field.
  
• Previous experience invalidation activities within a regulated environment preferred (MedicalDevice, Pharmaceutical, or Manufacturing).