About the Opportunity
We are seeking a highly skilled CQV Equipment Engineer to join our team in Dublin, Ireland. The successful candidate will be responsible for developing and executing CQV testing documentation for Utilities in a Sterile Drug product facility.
Key Responsibilities:
* Development and execution of CQV testing documentation for Utilities
* Meeting key project deliverables for safety, CQV schedule, and quality of project-related documentation/electronic records for equipment and utilities assigned
* Ensuring Utilities are tested in compliance with good manufacturing practices, company policies, and EU & FDA regulations
* Ensuring non-GMP equipment Utilities are tested in compliance with project-related standards from a commissioning perspective
About You
The ideal candidate should possess a minimum of a BS qualification (Degree) in a scientific, technical, or engineering discipline and have a minimum of 5 years of experience with utility systems commissioning preferably in a sterile drug product facility.
A Stamp 1G or a Stamp 4 visa is required for applicants interested in contracting opportunities within the pharmaceutical sector in Ireland. Please note that we do not provide visa sponsorship.
Requirements:
* BS qualification (Degree) in a scientific, technical, or engineering discipline
* Minimum 5 years of experience with utility systems commissioning in a sterile drug product facility
* Stamp 1G or a Stamp 4 visa
Skills:
* Commissioning
* CQV
* API
* Pharmaceutical