💼 About This Role

You'll perform routine QC microbiology testing and environmental monitoring in a cGMP lentiviral vector manufacturing facility. Your work supports off-the-shelf cancer immunotherapy development at a cutting-edge biotech. This role is fully onsite in Louisville, CO.

🎯 What You'll Do

• Perform routine QC lab work including environmental monitoring and compendial testing
• Generate and revise QC documents per document management processes
• Assist in developing training materials and deliver training for QC programs
• Execute qualification/validation activities for lab equipment and systems

📋 Requirements

• Bachelor's degree in life science with 3-5 years cGMP QC experience
• Understanding of Operational Excellence/Continuous Improvement in regulated lab
• Passion for teamwork and commitment to a people-focused culture

✨ Nice to Have

• QC experience in an FDA-regulated cGMP manufacturing facility
• Previous clean room experience
• Experience in cell and gene therapy manufacturing or testing

🎁 Benefits & Perks

• 🏥 Medical, Dental, and Vision plans
• 💰 401k match up to 4%
• 🏖️ Generous PTO policy
• 🚆 Commuter benefits