💼 About This Role

You'll ensure therapeutic products meet quality standards in San Francisco. Your work directly impacts patient safety and regulatory compliance.

🎯 What You'll Do

• Develop and implement quality assurance protocols
• Conduct audits of manufacturing processes
• Analyze quality data to identify trends
• Collaborate with cross-functional teams on corrective actions

📋 Requirements

• Bachelor's degree in a life sciences field
• 2+ years of quality engineering experience in regulated industry
• Knowledge of GMP and FDA regulations

✨ Nice to Have

• Experience with Lean or Six Sigma methodologies
• Familiarity with electronic quality management systems

🎁 Benefits & Perks

• 🏥 Health insurance
• 🏖️ Paid time off
• 📈 401(k) matching