Remoto: Teletrabajo

OverviewSe anima a todos los posibles solicitantes a que se desplacen y lean la descripción completa del puesto antes de presentar su candidatura.In this role you lead MedTech Complaints implementations for Veeva’s customers, guiding transformation of complaints management processes and configuring Vault for enterprise use. You will partner with customers and cross-functional teams to translate requirements into scalable solutions that drive quality and regulatory compliance. The position supports a fast-moving, customer-centric Professional Services group and offers remote work within the EU/UK. You’ll play a key part in expanding adoption of Veeva Vault while advancing continuous improvement post-implementation.Compensaciones / BeneficiosRemote work availableWork Anywhere policyCompetitive total compensationOpportunity to influence integral MedTech implementationsCollaborative, inclusive cultureResponsabilidadesLead QMS Complaints implementation workstreams for MedTech Quality Management solutionsAct as primary liaison between implementation teams, customer stakeholders,



and third partiesAnalyze requirements and product features to develop adoption and enhancement roadmapsGuide customers in adopting Vault and industry best practices in post-implementation programsRequisitos principales5+ years in Complaints Management for Medical DeviceStrong understanding of FDA, EU MDR/IVDR requirements and ReportingKnowledge of CAPA, Nonconformance and Risk Management relationshipsFamiliarity with ISO 13485 and 14971, FDA 21CFR parts 803, 820, 822, 806, EU GMP Annex 11Proven ability to work independently and in teams in fast-moving environmentsGood understanding of SaaS xcgbitx and GxP principlesAbility to translate business requirements into creative solutionsExcellent verbal and written communication skillsExperience in Life Sciences Quality, Manufacturing, or Healthcare spacesExperience with Data or Content Management applicationsexcellent communicationteam collaborationability to work independently in dynamic environmentsComplaints Management for Medical DeviceRegulatory knowledge (FDA/EU MDR/IVDR)CAPA, Nonconformance, Risk Management

📌 Senior Consultant - Medtech QMS Complaints - españa
🏢 Jobrapido
📍 España