🛠 Tech Stack

💼 About This Role

You'll lead CQV of critical utility systems for a pharmaceutical facility, ensuring GMP compliance. You'll collaborate with multidisciplinary teams and support audits. This role offers hands-on validation work in a project-driven environment.

🎯 What You'll Do

• Design, operate, and maintain utility systems (WFI, purified water, cleaning steam).
• Perform system validation and support IQ/OQ/PQ activities.
• Monitor performance, troubleshoot issues, and implement improvements.
• Collaborate with production, quality, and engineering teams.
• Support audits and regulatory inspections.

📋 Requirements

• 5-8 years of relevant experience in pharmaceutical utilities.
• Proven CQV experience with clean and black utilities.
• Knowledge of GMP and regulatory requirements.
• Ability to work independently in a project-driven environment.

✨ Nice to Have

• Familiarity with Kneat e-validation system.
• Experience with HVAC and process gases.