💼 About This Role

You'll perform commissioning and qualification (CQV) activities for a pharmaceutical client, ensuring safety and compliance. Your efforts will directly impact project schedules and regulatory success. This role offers the chance to work with a top-tier professional services firm.

🎯 What You'll Do

• Perform CQV activities with a focus on safety
• Generate and review C&Q procedures and documentation
• Support execution of FATs, IQ, OQ, and PQ
• Coordinate with contractors and equipment vendors

📋 Requirements

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

✨ Nice to Have

• Relevant experience can substitute for education
• Strong problem-solving abilities
• Customer-focused mindset