Engineering - IE_Commissioning Engineer - CQV

Dublin, Ireland (Onsite) Contract: 12 months

Specifically experience with CQ of Single Use Mixers & TCUs, Utility Panels & Filtration Systems (TFF), Autoclaves, Parts Washers and Powder Handling equipment such as Blenders and Jet Mills.

Join our team as a CQV Engineer supporting the commissioning and qualification of equipment within a Sterile Drug Product manufacturing facility. You will work with cross-functional teams to ensure systems are delivered safely, compliantly, and on schedule in line with GMP, EU, and FDA regulations.

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• Develop and execute CQV documentation and testing for assigned equipment.
  
• Support commissioning, qualification, and validation activities across the project lifecycle.
  
• Ensure testing complies with GMP, company procedures, and regulatory standards.
  
• Participate in Factory Acceptance Testing (FAT) and integrate results into qualification activities.
  
• Manage deviations and CQV risks, ensuring proper documentation and resolution.
  
• Collaborate with project teams to deliver high-quality CQV outcomes on time and within scope.
  

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• Bachelor's degree in Engineering, Science, or a related technical discipline.
  
• 5+ years of pharmaceutical industry experience.
  
• Experience working with sterile drug product manufacturing equipment and automation.
  
• Strong documentation, communication, and problem-solving skills.
  
• Ability to work independently and within cross-functional project teams.
  

Ready to contribute to the delivery of critical pharmaceutical manufacturing projects? xcfaprz Apply today and join a high-performing CQV team.

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