💼 About This Role

You'll perform supplier quality audits at various sites in western Canada, including a 3-day audit near Vancouver. These 1-2 day audits ensure quality in pharmaceutical, medical device, and biologics supply chains. You have flexibility to accept or reject assignments based on your availability.

🎯 What You'll Do

• Perform supplier audits at various sites within your region
• Coordinate, prepare, execute, and deliver supplier audits
• Write audit reports in accordance with client specifications
• Respond to Content team regarding edits to audit reports

📋 Requirements

• 4+ years of hands-on audit experience in pharmaceutical/medical device/biologics
• Lead auditor in at least 10 audits
• Direct audit experience to ISO 13485 and 21 CFR part 820
• Willingness to travel regionally

✨ Nice to Have

• Direct audit experience to 21 CFR part 210/211, EU Vol 4, and ISO 9001
• ISO certifications are a plus

🎁 Benefits & Perks

• ✈️ Travel opportunities within western Canada
• 📅 Flexible schedule - accept or reject assignments

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Application· 1 day
2. 2Phone Screen· 30 min
3. 3Offer· 1 day