💼 About This Role

You'll perform supplier quality audits at various sites in the Beijing area for a leading provider of managed supplier quality services. Your core impact is ensuring compliance with regulatory standards across pharmaceutical, medical device, and biologics industries. This contract role offers flexibility to accept assignments based on your availability.

🎯 What You'll Do

• Perform supplier audits at sites within your region
• Assure quality in supply chains of pharma/device clients
• Coordinate and execute supplier audits per client schedule
• Write audit reports in accordance with client specifications

📋 Requirements

• 5+ years of hands-on audit experience in pharma/medical device/biologics
• Lead auditor in at least 10 audits
• Direct audit experience with 21 CFR part 210/211, EU Vol 4, China GMP, 21 CFR part 820, and ISO 13485
• Willingness to travel regionally

✨ Nice to Have

• Direct audit experience with ISO 17025, ISO 15378, IPEC, ICH Q7 and/or Canada GMP
• ISO certifications are a plus

🎁 Benefits & Perks

• ✈️ Flexible assignment scheduling

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Technical interview· 60 min
3. 3Offer· 30 min