Quality meets innovation. Are you ready to validate the future? What’s in it for you? Hybrid work setup → 2 days remote, 3 in the office Fixed-term contract → 1 year with real impact from day one Competitive salary → €41,000 to €45,000 per year Work hours → 8:00 AM – 5:30 PM, work-life balance matters Your mission : Implement and execute SOP CSV 418 Validate software under FDA & EU regulations ( 21 CFR Part 11/820, ISO 13485:2016 ) Design and test procedures aligned with regulated standards Create validation specs, lead reviews, and ensure quality every step of the way Collaborate cross-functionally to shape internal validation processes What you bring: A degree in Computer Science, Life Sciences, Engineering, or similar 3 years in the pharma or medical device world Strong command of CSV, QA, risk management, and regulatory compliance Hands-on experience with IQ/OQ/PQ validation steps Fluency in English (Spanish or German is a plus!) If you're someone who gets excited about making systems safer, smarter, and fully compliant, let’s talk. This isn’t just another role it’s your chance to engineer quality that truly matters. Tag someone who should see this or apply now. Let's build quality into everything together.