Dublin, Ireland (Onsite) Contract: 12 months
Must-Have Equipment Experience
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? Apply today and join a high-performing CQV team.
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