💼 About This Role

You'll lead the Quality organization in a pharmaceutical manufacturing setting, overseeing GMP compliance and continuous improvement. Your core impact is ensuring high standards of quality across operations and managing regulatory audits. This role stands out for its focus on oral solid dosage manufacturing capabilities.

🎯 What You'll Do

• Lead Quality Assurance and Quality Control teams
• Oversee the Quality Management System (QMS) for GMP compliance
• Manage regulatory inspections and customer audits
• Develop and administer departmental budgets and resource plans

📋 Requirements

• 15+ years progressive leadership in pharmaceutical Quality
• 10+ years in Director-level role with commercial/clinical functions
• Expert knowledge of cGMP and FDA regulatory requirements

✨ Nice to Have

• Master's degree (MBA, MS) preferred
• Experience with spray drying technology for pharmaceuticals

🎁 Benefits & Perks

• 🏖️ Leadership role in a growing CDMO
• 🏢 Onsite in Bend, Oregon
• 📈 Strategic impact on quality systems and compliance

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Panel Interview· 90 min