Quality Associate

QRC Group; Aibonito (PR); On-site; USD 42,000 - 64,000; Full time

Job summary

QRC Group in Aibonito, Puerto Rico is seeking a Quality Associate to support and maintain quality systems in a regulated manufacturing environment. The successful candidate will review and manage quality documentation, participate in investigations and CAPAs, and provide quality support to manufacturing operations to ensure compliance with GMP and regulatory requirements.

This role requires strong attention to detail, a commitment to continuous improvement, and the ability to collaborate with

Qualifications

• 3 to 5 years of experience in process quality areas.
• Experience in regulated manufacturing environments.
• Knowledge of GMP documentation.
• Experience with quality systems, investigations, documentation, and support of manufacturing processes.

Responsibilities

• Review and manage quality documentation.
• Participate in investigations and CAPAs.
• Provide quality support to manufacturing operations.
• Help ensure products and processes meet quality and regulatory requirements.

Skills

GMP knowledge

CAPA investigations

Quality systems

Documentation support

Job description

Aibonito, Puerto Rico | Posted on 07/27/2026

We are seeking a Quality Associate to support and maintain quality systems, ensuring compliance with GMP regulations, industry standards, and company policies within a regulated manufacturing environment. The successful candidate will be responsible for reviewing and managing quality documentation, participating in investigations and corrective and preventive actions (CAPAs), providing quality support to manufacturing operations, and helping ensure that products, processes, and systems consistently meet established quality and regulatory requirements. This role requires strong attention to detail, a commitment to continuous improvement, and the ability to collaborate effectively with cross-functional teams to drive quality excellence and operational compliance.

Requirements

• 3 to 5 years of experience in process quality areas.
  
• Experience in regulated manufacturing environments.
  
• Knowledge of GMP documentation.
  
• Experience with quality systems, investigations, documentation, and support of manufacturing processes.