CQV Engineer ( Production)

Your new company

At Hays Specialist Recruitment we have a great opportunity for a CQV Engineer to join our Biopharmaceutical client in Dublin on an initial 14-month contract.In association with the CQV Lead prepare and execute the site commissioning and validation testing for equipment utilities at Drug Product Facility in alignment with site and global procedures.

Your new role

• Development and execution of CQV testing documentation for Equipment for the Sterile Drug product facility.
• Responsible for meeting key project deliverables for safety, CQV schedule and quality of project-related documentation / electronic records for equipment assigned.
• Responsible for ensuring GMP equipment is tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
• Responsible for ensuring that all non-GMP equipment is tested in compliance with project-related standards from a commissioning perspective.

What you'll need to succeed