💼 About This Role

You'll perform supplier quality audits at pharmaceutical sites in the Midwest, ensuring regulatory compliance with FDA and ISO standards. You'll have flexibility to choose assignments based on your availability.

🎯 What You'll Do

• Perform supplier audits at various sites within your region
• Assure quality in pharmaceutical supply chains
• Coordinate and execute supplier audits per client schedule
• Write audit reports to client specifications

📋 Requirements

• 5+ years of hands-on audit experience in pharma/device/biologics
• Lead auditor in at least 10 audits
• Direct audit experience with 21 CFR part 210/211 and ISO 9001
• Willingness to travel regionally

✨ Nice to Have

• Audit experience with ISO 17025, 21 CFR part 58, IPEC, ICH Q7, or ISO 13485
• ISO certifications

🎁 Benefits & Perks

• 💰 Flexible schedule - choose assignments that fit your availability
• ✈️ Travel opportunities within the Midwest region

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Interview with Hiring Manager· 45 min
3. 3Offer· N/A

🚩 Heads Up

• Listing mentions multiple industries (pharma, medical device, cosmetics, biologics, animal health) which may dilute focus
• Requires 5+ years audit experience but also 'ability to adapt to new technology and software' - mismatch with senior level