Descripción de la oferta
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 / BeneficiosHybrid modelFlexible scheduleBenefits packagePermanent contract
ResponsabilidadesCollect and review documentation to prepare and execute auditsDefine and coordinate audit agenda aligned with objectives and stakeholdersPrepare audit-related documents including checklists and working papersConduct Corporate Quality Audits per plan, scope, and timelinesPrepare comprehensive audit reports with findings and improvement opportunitiesEvaluate and classify findings with practical recommendationsFollow up on CAPAs and monitor implementation and effectivenessSupport management and reporting of quality indicators and KPIsCollaborate with internal stakeholders to promote continuous improvement and complianceEnsure adherence to corporate quality standards and regulatory requirements throughout audit processes
Requisitos principales3–5 years of GDP experience in pharmaceutical industryLife Sciences Degree (Pharmacy, Biology, Chemistry, Biotechnology) or Engineering Degree (Chemical or Industrial) or 10 years experienceAuditing GxP experience desiredStrong analytical and communication skillsWillingness to travel ~30%Advanced English level (written and spoken)analytical thinkingstrong communicationcross-functional collaborationGDP/GxP auditingCAPA managementaudit planning and reporting
