Experteer Overview
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 / Beneficios
• Lead QMS Complaints implementation workstreams for MedTech Quality Management solutions
• Act as primary liaison between implementation teams, customer stakeholders, and third parties
• Analyze requirements and product features to develop adoption and enhancement roadmaps
• Guide customers in adopting Vault and industry best practices in post-implementation programs

Responsabilidades




• 5+ years in Complaints Management for Medical Device
• Strong understanding of FDA, EU MDR/IVDR requirements and Reporting
• Knowledge of CAPA, Nonconformance and Risk Management relationships
• Familiarity with ISO 13485 and 14971, FDA 21CFR parts 803, 820, 822, 806, EU GMP Annex 11
• Proven ability to work independently and in teams in fast-moving environments
• Good understanding of SaaS and GxP principles
• Ability to translate business requirements into creative solutions
• Excellent verbal and written communication skills
• Experience in Life Sciences Quality, Manufacturing, or Healthcare spaces
• Experience with Data or Content Management applications

Requisitos principales
• Remote work available
• Work Anywhere policy
• Competitive total compensation
• Opportunity to influence integral MedTech implementations
• Collaborative, inclusive culture

📌 Senior Consultant - Medtech QMS Complaints (España)
🏢 Veeva Systems
📍 España