Overview

As QA Officer you ensure quality oversight across GMP activities at the site. You will support validation/qualification efforts, manage quality documentation, and supervise batch release activities. Working in shifts, you contribute to audits, inspections, and continuous improvement of the local quality system.

This role offers exposure to cross-functional coordination and regulatory compliance in a global pharma environment. You will partner with QP and QA colleagues to safeguard product quality and compliance.

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

Responsabilidades Oversee hygiene and facility conditions

Support validation/qualification status, training, and quality documentation

Responsible for provisional batch release

Collaborate with QA officers to supervise production and QC activities

Archive and manage GMP documentation, review batch records, close batches





Maintain local quality system per GMP and corporate guidelines

Assist in batch release documents with QP

Contribute to drafting GMP documentation and batch documentation

Support data compilation for Product Reviews, monitor investigations and corrective actions

Participate in self-inspections and external audits

Ensure quality oversight during GMP activities per standards in manufacturing, QC, distribution and quality processes

Requisitos principales 1+ years of experience in a Quality department

Strong affinity with and awareness of quality issues

Good organizational skills with attention to detail

Solid knowledge of GMP quality systems and basic regulatory requirements

Fluent in English (spoken and written)

Collaboration

Leadership

Operational excellence

GMP knowledge

Quality system understanding

Regulatory compliance awareness

📌 Quality Assurance Officer Operations (Zaragoza)
🏢 Novartis
📍 Zaragoza