OverviewIn this role you will ensure commercial medicinal products meet manufacturing, testing, and distribution requirements under current legislation and internal procedures.

You will review samples and documentation and manage release for distribution, operating within a cross-functional quality environment.

You will support GxP compliance and the Quality Management System, contributing to safe and compliant product supply.

This position offers exposure to EU regulatory activities and batch certification processes in a integral pharma setting.

Compensaciones / Beneficiosinsurance plans retirement plans wellbeing resources global recognition programs flexible and hybrid working options minimum of 14 weeks paid parental leave

ResponsabilidadesPerform batch documentation review prior to release by the QP

Initiate and obtain the EU Batch Certificate for centrally authorized products

Assess transport of products and evaluate temperature excursions





Manage urgent requests and releases

Manage reconditioning of commercial batches in line with GMPs

Ensure implementation of SLC with Supply, DRA, and related departments

Report monthly indicators and maintain documentation and sample archives

Review samples and related documentation

Ensure overall GxP compliance and compliance with Novartis Quality Management Systems

Requisitos principales1+ years of experience in Quality Assurance and/or Quality Control

Strong knowledge of GMPs and pharmaceutical manufacturing processes

Native Spanish and good level of English

GMP knowledge

Quality Assurance/Quality Control

Batch documentation review

Release for distribution processes

EU Batch Certificate initiation and handling

SLC implementation collaboration with Supply, DRA, and other departments

📌 Quality Assurance Release Officer - Barcelona
🏢 Novartis
📍 Barcelona