💼 About This Role

You'll perform commissioning, qualification, and validation activities for a pharmaceutical/life sciences client. Your work will directly impact regulatory compliance and product safety. You'll coordinate with vendors and contractors to execute testing.

🎯 What You'll Do

• Perform CQV activities with strong safety focus
• Support generation and review of C&Q procedures
• Coordinate with contractors and equipment vendors for testing
• Track and report progress of CQV efforts

📋 Requirements

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

✨ Nice to Have

• Outstanding oral and written communication skills
• Strong problem-solving abilities
• Customer-focused mindset

🚩 Heads Up

• Vague company culture description unrelated to role
• Required travel may be excessive for some candidates