💼 About This Role

You'll perform supplier quality audits at pharmaceutical and medical device sites in Japan, ensuring compliance with regulatory standards. This contract role offers flexibility to accept assignments based on your availability.

🎯 What You'll Do

• Perform supplier audits at various sites within your region.
• Assure quality in supply chains for pharmaceutical and medical device clients.
• Coordinate, prepare, execute, and deliver supplier audits per schedule.
• Write audit reports in accordance with client specifications.

📋 Requirements

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

✨ Nice to Have

• Direct audit experience with ISO 17025, ISO 15378, IPEC GDP, ICH Q7, or Canada GMP.
• ISO certifications.

🎁 Benefits & Perks

• ✈️ Travel opportunities within Japan.
• 📅 Flexible schedule with accept/reject assignments.
• 🔧 Contract work with diverse clients.

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 1 hour
3. 3Offer· 1 week