Quality Validation Specialist (CSV)

Overview 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.

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