💼 About This Role

You'll lead CQV projects for bio-pharma systems, managing scope, schedule, and budget for teams of engineers. Your core impact is delivering complex life science projects with budgets over $1M. You'll also mentor teams and drive risk assessments and qualifications.

🎯 What You'll Do

• Lead budget review and daily team huddles
• Review summary reports and write protocols
• Support field execution of commissioning and qualification
• Manage scope, schedule, and budget for projects

📋 Requirements

• BS in science or engineering or equivalent experience
• 8-12 years experience commissioning and qualifying bio-pharma systems
• 3+ years managing life science projects with budgets over $1M
• Able to work in the US without sponsorship

✨ Nice to Have

• Experience with risk assessments and qualification protocols
• Experience with CIP/SIP
• PMP certification

🎁 Benefits & Perks

• 🏖️ Up to 15% retirement contribution
• 🏖️ 24 days PTO and 5 sick days per year
• 🏥 Low-cost health insurance
• 📚 Financial support for professional education
• 🛡️ 70% long term disability paid by company

🚩 Heads Up

• Requires 8-12 years experience but also 3+ years as PM (redundant)
• Mentions 'desktop PMs need not apply' implying on-site requirement