💼 About This Role

You'll lead complex contract negotiations with CDMOs and suppliers for a late-stage oncology company. Your work will directly impact drug development and commercialization by structuring agreements that ensure supply continuity. This role offers deep collaboration with technical and quality teams in a fast-paced biotech environment.

🎯 What You'll Do

• Draft and negotiate CDMO master services agreements and work orders
• Advise on legal risks related to GMP manufacturing and supply continuity
• Partner with Technical Operations, Quality, and Supply Chain teams
• Develop contracting templates and internal processes

📋 Requirements

• J.D. from an accredited law school
• 10+ years of relevant legal experience with contract manufacturing focus
• Active license to practice law in at least one U.S. jurisdiction
• Experience in biotech or pharmaceutical industry

✨ Nice to Have

• In-house experience at a biotech or pharmaceutical company
• Familiarity with global manufacturing arrangements and international vendors
• Experience supporting clinical-stage and/or commercial manufacturing

🎁 Benefits & Perks

• 💰 Competitive Cash Compensation
• 📈 Robust Equity Awards
• 🏥 Strong Benefits
• 📚 Learning and Development Opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Interview with Hiring Manager· 60 min
3. 3Interview with Legal Team· 60 min