Your new company

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

• Demonstratable 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.

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.