Description
Global Biophamaceutical plant, based in Dublin, has a contract requirement for an experienced QAV Consultant to work closely with the CQV Team on site.Having recently invested in a new site, which will become a Global Headquarters operational by 2016, we are looking for an experienced Quality Assurance Validation Consultant with previous ASTME2500 experience and ideally have worked within a Drug Substance /Sterile environment.
Candidates must have extensive Quality Assurance and completions experience, co-ordinating quality objectives through design, commissioning, validation/verification through to handover and operations. You will be required to review and approve documentation such as risk assessments & CQV ensuring that all documentation is compliant and in accordance with the FDA & EU, cGMP standards
Excellent communication skills will be required with the ability to work independently.