💼 About This Role

You'll lead mid- to large-scale life sciences projects, guiding commissioning, qualification, and validation activities from design to delivery. You'll collaborate with recognized subject-matter experts to ensure safe, compliant, and efficient project execution. This role offers employee ownership and a collaborative culture.

🎯 What You'll Do

• Provide cGMP leadership to integrate CQV services
• Manage mid-sized to large projects involving process equipment
• Lead design reviews, equipment installation, and site acceptance
• Write, review, and approve CQV documents per 21 CFR

📋 Requirements

• BS or MS in engineering or science
• 8+ years CQV experience in life sciences
• Knowledge of EU regulatory requirements and cGMP
• Experience managing CQV deliverables across projects

✨ Nice to Have

• Complex or multi-site project coordination
• Leading international project teams

🎁 Benefits & Perks

• 💰 Employee ownership
• 📚 Professional training and certifications
• 🌍 Global exposure on international projects
• 🤝 Collaborative culture