Job Description

Commissioning Engineer – CQV 

Location: Dublin, Ireland Onsite)

 Contract Duration: 12 Months

Are you a CQV pro ready to make a real impact in sterile pharmaceutical manufacturing? Join our team and lead the commissioning, qualification, and validation of cutting-edge equipment and utilities that ensure the highest quality for life-saving medicines.

Key Responsibilities

• Develop, execute, and review CQV documentation for clean utilities and sterile manufacturing equipment.
  
  
• Ensure all systems are GMP, EU & FDA compliant throughout commissioning and qualification.
  
  
• Plan, execute, and leverage FAT/SAT testing to support overall qualification.
  
  
• Identify, assess, and mitigate CQV risks, generating actionable plans to keep projects on track.
  
  
• Manage deviations and CAPAs for assigned equipment and utilities.
  
  
• Collaborate with cross-functional teams and contractors to deliver projects safely, on time, and within budget.
  
  
• Ensure training compliance and contribute to continuous improvement initiatives.
  
  
• Support the handover of qualified systems to operations, ensuring seamless integration into production.
  
  

Required Experience and Qualifications

• BS in Scientific, Technical, or Engineering discipline (required).
  
  
• 5+ years in pharmaceutical CQV, ideally with sterile drug product lines.
  
  
• Expertise in High Purity Water, Clean Steam, and Gas systems.
  
  
• Experience with electronic validation platforms (ValGenesis, Kneat).
  
  
• Strong communication and teamwork skills in matrix environments.
  
  

Take your CQV career to the next level – apply today!