Computer System Validation (CSV) Specialist

Computer System Validation (CSV) Specialist Do you want to contribute to cutting-edge projects in the Life Sciences while specializing in Computer Software Validation (CSV)? We’d love for you to join our expanding Software and Services division Join us! 🔍 Computer System Validation (CSV) Specialist 📍 Location : Hybrid 🕓 Type : Full-time QbD Group’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in Software Solutions. 💡 What’s in it for you? Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices Grow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise. Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences. A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued. 🏢 What you’ll be doing As a Software Validation Consultant, you will play a critical role in managing and overseeing project deliverables for a variety of cutting-edge applications, such as: Automated systems Software as a Medical Device (SaMD) Mobile apps From preparation and project design to implementation and follow-up , you will provide full-cycle support to clients, ensuring the successful delivery of projects. You will also contribute to the integration and implementation of our proprietary QbD quality management software at client sites. With your knowledge of data integrity and quality management , you will support companies across the Life Sciences, including pharmaceuticals, biotech, medical devices and healthcare—from large, established firms to the most innovative start-ups. 💪 What you bring You hold a master’s degree in a scientific or engineering field (e.g., bio-engineering, bioinformatics, industrial engineering, civil engineering, etc.). You have some experience in the Life Sciences industry or with software-related projects . You have a strong affinity with IT, software, and systems. You have knowledge of data integrity . You are detail-oriented, eager to learn, and adaptable to new challenges. You possess strong technical and project management skills. You are responsible, with a strong analytical mindset and excellent problem-solving abilities. 🫵 Who you are Our culture is driven by values If this sounds like you, you’ll fit right in: You’re resilient and tackle challenges with a positive mindset You’re curious and always up for learning something new You have a no non-sense approach honest, clear, respectful You’re innovative and bring ideas, not just opinions And above all, you’re serious about your work, but not too serious about yourself ✨ About us We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma. We believe in JPEG : Joy. Partnership. Going the Extra Mile. Getting Things Done. You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger. 📩 Interested? Let’s talk. Send us your CV and motivation letter. You could be the next one to join the QbD family Service Software Solutions & Services Role Software Validation Specialist Locations QbD Spain (Barcelona), QbD Wallonia, QbD Flanders (HQ) Remote status Hybrid