💼 About This Role

You'll develop CQV documentation and execute protocols for pharmaceutical facilities and utilities. You'll also coordinate small teams and contribute to project success. This role offers the chance to work with ISPE Baseline Guide 5 and gain experience in regulated environments.

🎯 What You'll Do

• Write and execute protocols for field verification
• Develop summary reports at client sites
• Plan and coordinate work for small teams
• Conduct walk-downs and troubleshooting

📋 Requirements

• Bachelor's degree in science or engineering
• 2-4 years experience in commissioning and qualification
• Familiarity with ISPE Baseline Guide 5 (preferred, but not required)

✨ Nice to Have

• Experience in facilities and equipment startup
• Knowledge of utilities (WFI, RO, HVAC)
• Experience in pharmaceutical manufacturing processes