💼 About This Role

You'll lead commissioning and qualification activities for life sciences projects, ensuring compliance with FDA regulations for clients like cutting-edge biotech firms.

🎯 What You'll Do

• Conduct and lead CQV team activities with safety focus.
• Manage C&Q documentation from SLIA to OQ completion.
• Prepare Qualification Summary Reports and RTM.
• Coordinate with contractors and vendors for testing.

📋 Requirements

• BS or MS in science or engineering field.
• 3+ years in CQV SME roles for life sciences.
• Proficient in life science manufacturing processes.
• Willingness to travel domestically and internationally.

✨ Nice to Have

• Clean Utilities/Filling experience.
• Experience with biotech, aseptic fill/finish, OSD, or Gene Therapy.

🎁 Benefits & Perks

• 🏢 Employee-owned company
• 📈 Growth opportunities
• 🎓 Hands-on certifications and training
• 🤝 Collaborative culture