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📍 Location
león
⏰ Job Type
Full-time
📅 Posted
June 11, 2026

About the Role

Experience: At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings

Position Overview

We are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight who is passionate about the industrialisation of new products.

General Responsibilities

Ensure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real-time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations.

Specific Responsibilities

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