💼 About This Role

You'll perform downstream manufacturing operations for AAV-based gene therapy products in a cGMP facility. You'll execute chromatography, filtration, and formulation steps while monitoring critical process parameters to ensure product quality. This role offers the chance to contribute to life-changing therapies in a state-of-the-art environment.

🎯 What You'll Do

• Perform chromatography, filtration, and viral vector formulation steps
• Prepare and operate purification equipment per SOPs
• Monitor process parameters and report deviations
• Assist in process validation and technology transfer

📋 Requirements

• Associate's degree in a scientific field or equivalent experience
• Experience in a laboratory or regulated manufacturing environment
• Ability to work flexible hours including evenings and weekends
• Ability to stand for extended periods in a cleanroom

✨ Nice to Have

• Knowledge of cGMP regulations
• Experience with AAV manufacturing
• Teamwork and communication skills

🎁 Benefits & Perks

• 🏖️ PTO and holidays
• 💰 Competitive compensation
• 🏥 Health insurance
• 📚 Training and development
• 🏢 State-of-the-art facility

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Onsite interview· 2 hours

🚩 Heads Up

• Job description includes vague duties and may change
• Requires flexibility including holidays and weekends