Validation Engineer/Molding

QRC Group; Aibonito (PR); On-site; USD 55,000 - 75,000; Full time

Job summary

QRC Group in Aibonito, Puerto Rico is seeking a Validation Specialist to support validation activities in the Injection Molding area. The selected candidate will assist in the execution, documentation, and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requirements.

The role involves collaboration with Manufacturing, Engineering, Quality, and Validation teams to meet project objectives and maintain cGMP-compliant documentation, while

Qualifications

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

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 the 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.

Education

Bachelor’s degree in Engineering, Life Sciences, or a related technical field

Job description

Aibonito, Puerto Rico | Posted on 06/29/2026

We are seeking a Validation Specialist to support validation activities within the Injection Molding area. The selected candidate will assist in the execution, documentation, and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requirements.

Key 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 the 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.

Requirements

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