💼 About This Role

You'll lead analytical method development and validation for gene therapy viral vectors under cGMP standards. Your work directly impacts the path to new cures by ensuring robust QC assays. You'll collaborate cross-functionally in a fast-growing company.

🎯 What You'll Do

• Lead analytical method development and validation for gene therapy products
• Direct method transfer from AD to QC lab under cGMP
• Supervise and train AD Associates and Technicians
• Support tech transfer of assays from clients to AD and to QC

📋 Requirements

• 5-6 years post-PhD or equivalent experience
• Expertise in potency assays for AAV vectors
• Expertise in ddPCR/qPCR and ELISA
• Direct line management experience

✨ Nice to Have

• Experience with biophysical characterization (HPLC, LC-MS, CE-SDS)
• CRO/CDMO experience in bioanalytical method development

🎁 Benefits & Perks

• 💰 Competitive annual salary $120k-$150k
• 🧬 Work on cutting-edge gene therapy
• 👥 Collaborative team environment
• 📈 Growth opportunities at a fast-growing company

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical interview· 60 min
4. 4Offer· N/A