Validation Engineer/Molding

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

Job summary

QRC Group is looking for a Validation Specialist to support validation activities within the Injection Molding area in Caguas, Puerto Rico. The ideal candidate will assist in the execution, documentation, and completion of validation projects, ensuring compliance with quality standards and regulatory requirements.

The role involves collaboration with Manufacturing, Engineering, and Quality teams, along with maintaining accurate documentation as per cGMP guidelines.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical field.
• Previous experience in validation activities within a regulated environment 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.
• Assist in the investigation and resolution of validation-related issues.
• Maintain accurate documentation in compliance with cGMP requirements.
• Participate in continuous improvement initiatives.

Skills

Validation protocols support

Data analysis and documentation

Collaboration with cross-functional teams

Issue investigation and resolution

cGMP compliance

Technical support

Education

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

Job description

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

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).