Engineering - IE_Commissioning Engineer - CQV

Next Generation View all jobs

  • Dublin
  • €70.00-80.00 per hour
  • Contract
  • Full-time
  • 27 days ago
  • Apply easily
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.Key Responsibilities
  • 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.
Requirements
  • 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?

Next Generation