Job Opportunity
We are seeking a C&Q Engineer to join our team in Dublin, dedicated to discovering and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
Key Responsibilities:
1. Collaborate with the Area CQV Lead to prepare and execute site commissioning and validation testing for equipment utilities, adhering to global procedures.
2. Develop and execute CQV testing documentation for Inspection Systems, including Syringe and Vial Automated Visual Inspection Equipment and Manual Inspection Booths for the Sterile Drug product facility.
3. Ensure key project deliverables for safety, CQV schedule, and quality of project-related documentation/electronic records for assigned equipment and utilities are met.
4. Verify GMP equipment testing complies with good manufacturing practices, company policies, and EU & FDA regulations.
5. Manage deviations associated with the assigned equipment and utilities.