Validation Officer

As a Validation Officer you will contribute to the establishment and the regular updating of the technical documentation (IVDR compliant).

Your responsibilities as validation officer include:

• Plan and perform validation protocols for new and existing products
• Analyze validation data and generate comprehensive reports
• Develop and maintain technical documentation related to validation and ensure that updates are available
• Stay up-to-date with evolving regulatory guidelines and best practices related to validation in the biotechnology sector
• Participate to risk assessments and change controls

Must have

• Master’s degree in science or engineering discipline (e.g., Chemistry, Biotechnologies, Chemical Engineering), or equivalent through experience
• Technical skills on immunoassays, molecular biology and/or mass spectrometry
• Strong analytical skills, well organized, studious, and precise
• You enjoy managing documentation: creating, reviewing and updating documents, and follow-up on their approval
• English : good knowledge (B2)

Nice to have

• Proven experience in validation activities within the biotechnology industry
• Knowledge on the ISO13485 and IVDR 2017/746 regulations are a plus

• 💹 The opportunity to really enjoy your work … you make the difference.
• 📈 A fast-growing environment. Your job evolves with the company.
• 🧬 We develop products for a healthier world. What matters is what we do.
• 🎨 A varied job. Days follow each other but are never alike …
• 👨‍👩‍👧‍👦 The chance to join a very enthusiastic team … collaborative and open-minded
• 💃 Fun team-building events
• ✅ Flexible hours. Flexible salary package.
• ⏲️ Permanent contract (38h/week)
• 🏞️ An exceptional working environment with a view over the woods of Sart-Tilman (Liège), as well as a south-facing terrace for afterwork events.
• 🍇 Free fruits at the office. 🥣 Free-Soup-Tuesdays