💼 About This Role

You'll perform commissioning, qualification, and validation activities for pharmaceutical clients. You'll ensure GMP compliance and equipment qualification while managing project schedules. This role offers opportunities for travel across the U.S. and internationally.

🎯 What You'll Do

• Execute CQV activities with safety focus
• Generate and review C&Q procedures for client projects
• Support design reviews, FATs, IQ, OQ, and PQ
• Coordinate with contractors and equipment vendors

📋 Requirements

• Bachelor's degree in Engineering, Chemistry, or Life Sciences
• 3+ years experience in Pharmaceutical/Life Sciences
• Experience in a GMP environment
• Willingness to travel throughout U.S. and internationally

✨ Nice to Have

• Outstanding communication skills
• Problem-solving abilities
• Customer-focused mindset