Overview

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At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We’re dedicated to revolutionizing science and healthcare for the better, with thousands of employees across six continents. Collaboration is our greatest strength, and we are always striving to identify talented individuals to join our exceptional teams.

About The Opportunity
Join QIAGEN as a Validation Engineer and contribute to ensuring the quality, safety, and compliance of our manufacturing processes and equipment. In this role, you will lead validation activities for injection molding tools and processes across their lifecycle, working closely with cross‑functional teams to maintain compliance with general regulatory standards such as ISO 13485 and GMP.

This is an onsite based role at QIAGEN Barcelona.

Your tasks include

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- Planning, executing, and documenting validation activities (DQ, IQ, OQ, PQ) for injection molding tools, equipment,



and manufacturing processes
- Developing and maintaining validation plans, protocols, and reports in line with GMP and internal quality standards
- Ensuring compliance with regulatory requirements (e.g., ISO 13485, GMP) throughout the product lifecycle
- Managing revalidation activities and assessing the impact of technical changes on validated systems
- Investigating deviations, non‑conformities, and out‑of‑specification results, including conducting root cause analysis and implementing CAPAs
- Collaborating with Quality Assurance, R&D;, and external partners to align validation strategies
- Reviewing and approving technical documentation, including specifications, risk analyses (FMEA), and change requests
- Supporting audits and inspections by providing validation documentation and technical expertise

Your profile

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- Degree in Engineering (e.g., Plastics, Mechanical, or Process Engineering)

📌 Validation Engineer (Barcelona)
🏢 Qiagen
📍 Barcelona