CQV Engineer Opportunity
At our client site in Dublin, we are seeking a skilled CQV Engineer to join their team on an initial 14-month contract. In association with the CQV Lead, this engineer will be responsible for preparing and executing site commissioning and validation testing for equipment utilities at the Drug Product Facility.
Your Key Responsibilities
* Develop and execute CQV testing documentation for Equipment at the Sterile Drug product facility.
* Meet key project deliverables for safety, CQV schedule, and quality of project-related documentation/electronic records for assigned equipment.
* E nsure that all GMP equipment is tested in compliance with good manufacturing practices, company policies, and EU & FDA regulations.
* Ensure that all non-GMP equipment is tested in compliance with project-related standards from a commissioning perspective.
What You Need to Succeed
* Demonstrate effective execution of the CQV testing approach assigned from initiation to completion.
* Have experience in the CQV project lifecycle from design through to C&Q and handover.
* Showcase ability to work as part of a diverse team of CQV professionals/contractors to deliver tasks safely, with quality focus, on time, and within budget.
* Exhibit experience in CQV of Drug Substance/Drug product sterile manufacturing equipment with integrated automation.