💼 About This Role

You'll develop documentation and execute protocols for commissioning and qualification at pharmaceutical client sites. You'll support facilities, utilities, and equipment startup in a regulated environment. This role offers hands-on field verification and small team leadership opportunities.

🎯 What You'll Do

• Develop CQV documentation including protocols and reports
• Write and execute field verification protocols at client sites
• Plan and coordinate work for small teams
• Direct teams during document development and execution

📋 Requirements

• Bachelor's degree in science or engineering
• 2–4 years of experience in commissioning and qualification in a regulated industry
• Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus
• Experience with facilities and equipment startup and troubleshooting

✨ Nice to Have

• Experience with utilities (WFI, RO, HVAC)
• Upstream/downstream processing knowledge
• Building automation experience