Your new company

Your new role

• Development and execution of CQV testing documentation for Utilities 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 and utilities.
• Responsible for ensuring utilities are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
• Responsible for ensuring that all non-GMP equipment utilities are tested in compliance with project-related standards from a commissioning perspective.

What you'll need to succeed

• 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 and Utilities with integrated automation platforms.
• Specific experience with the CQV preparation and execution for black utility systems, including compressed air plant steam, process waste, chilled water.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.