Join Our Biopharmaceutical Client
We are seeking a skilled CQV Engineer to join our team on an initial 16-month contract in Dublin. As part of this role, you will be responsible for ensuring the quality and safety of our Sterile Drug product facility.
About the Role
* Develop and execute CQV testing documentation for Utilities in compliance with good manufacturing practices and regulatory requirements.
* Meet key project deliverables for safety, schedule, and quality of project-related documentation and electronic records.
* Ensure utilities are tested in accordance with company policies, EU, and FDA regulations.
Your Background
* A minimum of a BS qualification (Degree) in a scientific, technical, or engineering discipline.
* A minimum of 5 years of experience within the pharmaceutical industry with familiarity with utility systems commissioning.
* CQV project lifecycle experience from design through to C&Q and handover.
* Demonstrable experience working as part of a diverse team to deliver tasks safely, with quality focus, on time, and within budget.
* Experience in CQV of Drug Substance/Drug product sterile manufacturing equipment and Utilities with integrated automation platforms.
What You'll Need to Succeed
* Capacity to effectively execute the CQV testing approach assigned from initiation to completion.
* Specific experience with the CQV preparation and execution for black utility systems, including compressed air plant steam, process waste, chilled water.