Overview 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. From our entrepreneurial roots to our current general presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams. We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. At QIAGEN, every day is an opportunity to make a real-life impact. Join us, grow with us, and together, let's shape the future of biological discovery. About the opportunityJoin 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 global regulatory standards such as ISO 13485 and GMP.This is an onsite based role at QIAGEN Barcelona.Please send your CV in EnglishYour tasks includePlanning, executing, and documenting validation activities (DQ, IQ, OQ, PQ) for injection molding tools, equipment, and manufacturing processesDeveloping and maintaining validation plans, protocols, and reports in line with GMP and internal quality standardsEnsuring compliance with regulatory requirements (e.g., ISO 13485, GMP) throughout the product lifecycleManaging revalidation activities and assessing the impact of technical changes on validated systemsInvestigating deviations, non-conformities, and out-of-specification results, including conducting root cause analysis and implementing CAPAsCollabora
📌 Technisch engineer. (España)
🏢 Qiagen
📍 España