💼 About This Role

You'll perform supplier quality audits at various pharmaceutical sites in Japan, with flexibility to accept assignments based on your availability. Your work ensures quality in global supply chains for top clients. This contract role offers rapid on-site engagement in Japan.

🎯 What You'll Do

• Perform supplier audits at various sites in Japan.
• Coordinate and execute audits per client schedule.
• Write audit reports in accordance with client specifications.
• Respond to content team regarding audit report edits.

📋 Requirements

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

✨ Nice to Have

• Direct audit experience to ISO 17025 or ISO 15378.
• ISO certifications are a plus.

🎁 Benefits & Perks

• ✈️ Travel Flexibility – Accept assignments based on your availability.
• 📋 Contract Role – Work on multiple short-term audits.