Experteer Overview
In this role, you contribute to ensuring quality, compliance, and reliability of products and processes within a regulated environment. You will support validation activities aligned with FDA regulations and ISO 13485, collaborating with cross-functional teams to drive continuous improvement. The position is onsite in Barcelona, offering hands-on exposure to IQ/OQ/PQ, CAPA, and documentation across equipment, software, and processes. You’ll help maintain robust validation records and support deviation handling. This is a great chance to shape quality in a global life sciences leader.

Compensaciones / Ventajas
• Support validation and qualification activities (IQ/OQ/PQ)
• Validate products, processes, equipment, utilities, software, and cleaning procedures
• Review and maintain validation documentation per SOPs/regulatory requirements
• Analyze protocol results and support CAPA implementation




• Verify calibration and performance of monitoring/measurement equipment
• Prepare validation reports and related documentation
• Support deviation handling and proper validation documentation

Responsabilidades
• Degree in Life Sciences, Engineering, or related field
• 1+ year in a regulated QA/validation environment (pharma, healthcare, medical devices or IVD)
• Experience writing/reviewing validation protocols (IQ/OQ/PQ)
• Familiarity with FDA regulations and ISO 13485 (advantage)
• Fluent in Spanish and English (written and spoken)
• Strong attention to detail with a compliant working approach
• Proficient in MS Office

Requisitos principales
• Meal voucher
• Health Insurance
• Bonus/Commission
• Referral Program
• Employee Assistance Program

📌 Validation Specialist (Barcelona)
🏢 Qiagen
📍 Barcelona