💼 About This Role

You'll lead supplier audits in pharmaceutical and regulated manufacturing environments for a global quality services leader. Your work ensures compliance with 21 CFR 210/211, EU GMP, and other standards.

🎯 What You'll Do

• Lead external supplier audits independently
• Audit quality systems, manufacturing controls, and documentation
• Prepare detailed audit reports and communicate findings
• Support corrective action reviews and follow-up activities

📋 Requirements

• 15+ years in Quality in pharmaceutical or regulated industries
• 5+ years performing audits as a lead auditor
• Experience with 21 CFR 210/211, EU GMP Vol. 4, or Canada GMP
• Willingness to travel throughout Southern California

✨ Nice to Have

• Experience with ISO 17025
• Experience auditing packaging or warehousing
• Knowledge of Food or Animal Health standards

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical Audit Discussion· 60 min