Description
QAV ConsultantA major global biopharmaceutical client is looking for a QAV Consultant to join the QA team on a new, state of the art filling line, based in West Ireland. This opportunity is to start ASAP with the contract lasting from 6-9 months. The QAV requires previous experience in reviewing Validation documentation and ideally experience in Filling and Sterile environments.
Main responsibilities
- Perform QA reviews on Validation/Qualification documentation for both the C&Q and Validation programmes
- Complete any project change requests
- Carry out deviation reviews when necessary
Key Skill Requirements
- Prior experience in reviewing Validation documentation
- Ideally have a background in Filling and Sterile environments
- Past experience with the following pieces of equipment:- Depyrogenation tunnels, Vial washers, Filling machines, Inspection machines, Syringe filling machines and Labelling machines
- Able to present information clearly and concisely in verbal and written form
- Good with people at all levels and a team player
This is an excellent opportunity to work with one of the most innovative Companies in the World! Please do get in touch for more information.