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CQV Engineer ( Production)
hays-gcj-v4-pd-onlineDublin North30+ days ago
Job descriptionDemonstratable capacity to effectively execute the CQV testing approach assigned from initiation to completion. CQV project lifecycle experience from design through to C&Q and handover. Demonstrable experience of performing as part of a diverse team of CQV professionals / contractors to deliver on tasks safely, with quality focus, on time and within budget. Experience in CQV of Drug Substance / Drug product sterile manufacturing equipment with integrated automation.
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
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Cqv Engineer • Dublin North