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 general life sciences leader.Compensaciones / Beneficios
- 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 documentationResponsabilidades
- 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 OfficeRequisitos principales
- Meal voucher
- Health Insurance
- Bonus/Commission
- Referral Program
- Employee Assistance Program

📌 Validation Specialist (Barcelona)
🏢 Qiagen
📍 Barcelona