💼 About This Role

You'll lead commissioning and qualification of bioreactor systems for a large-scale biopharma project. You'll ensure equipment meets GMP standards. This role offers hands-on work with cutting-edge bioprocess equipment.

🎯 What You'll Do

• Lead full lifecycle C&Q activities for process equipment
• Commission and qualify bioreactor systems
• Support downstream filtration and concentration systems
• Review and execute C&Q documentation

📋 Requirements

• Degree in Engineering or related discipline
• 5+ years in Commissioning & Qualification
• GMP and FDA/EMA regulatory knowledge
• Hands-on bioprocess and bioreactor experience

✨ Nice to Have

• Strong documentation and communication skills
• Experience with automation or validation