💼 About This Role

You'll implement quality assurance plans and lead regulatory compliance audits for a global clinical research organization. Your core impact is ensuring products and services meet ICH GCP standards while supporting continuous improvement.

🎯 What You'll Do

• Implement QA plans and processes for product/service quality.
• Conduct internal audits, vendor assessments, and site audits.
• Develop and maintain Quality System documents (policies, procedures).
• Train and oversee junior QA staff.

📋 Requirements

• undergraduate degree with 4-6 years experience or college diploma with 7-9 years.
• ICH GCP knowledge and global clinical research regulations.
• Clinical Quality Assurance or related specialty preferred.
• Strong analytical and problem-solving skills.

✨ Nice to Have

• Life Sciences or Clinical Research background.
• Knowledge of global privacy regulations.
• Experience with regulatory inspections.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Technical Interview· 60 min
3. 3Offer· 15 min