OverviewAs 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 / BeneficiosHybrid model

Adaptable schedule

Benefits package

Permanent contract

ResponsabilidadesCollect 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 principales3–5 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 (Barcelona)
🏢 Grifols
📍 Barcelona