Overview

As Corporate Quality Auditor at Grifols, you will perform corporate quality audits across Biopharma, Diagnostic and Healthcare units to assess GDP compliance and internal procedures. You will define audit agendas, prepare documentation, conduct audits, document findings, and suggest practical improvements. You will monitor CAPAs, support quality indicators, and collaborate with stakeholders to promote continuous compliance. This role offers cross-functional exposure and a chance to impact quality culture at scale.

Compensaciones / Beneficios

- Hybrid model
- Versátil schedule
- Benefits package
- Permanent contract

Responsabilidades

- Collect and review documentation to prepare and execute audits
- Define and coordinate audit agenda aligned with objectives and stakeholders
- Prepare audit-related documents including checklists and working papers
- Conduct Corporate Quality Audits per plan, scope, and timelines
- Prepare comprehensive audit reports with findings and improvement opportunities




- Evaluate and classify findings with practical recommendations
- Follow up on CAPAs and monitor implementation and effectiveness
- Support management and reporting of quality indicators and KPIs
- Collaborate with internal stakeholders to promote continuous improvement and compliance
- Ensure adherence to corporate quality standards and regulatory requirements throughout audit processes

Requisitos principales

- 3–5 years of GDP experience in pharmaceutical industry
- Life Sciences Degree (Pharmacy, Biology, Chemistry, Biotechnology) or Engineering Degree (Chemical or Industrial) or 10 years experience
- Auditing GxP experience desired
- Strong analytical and communication skills
- Willingness to travel ~30%
- Advanced English level (written and spoken)

- analytical thinking
- strong communication
- cross-functional collaboration
- GDP/GxP auditing
- CAPA management
- audit planning and reporting

📌 Pharma quality auditor (San Cugat del Vallés)
🏢 Grifols
📍 San Cugat del Vallés