Description
A Global Market Leading Pharmaceutical organisation is seeking an experienced Validation Engineer to take on a long term assignment in their state of the art sterile fill finish facility in Ireland. This is an excellent opportunity to work with an innovative industry leader during an exciting time.The Role:
*You will have a key role in ensuring the on-going validation compliance of equipment, systems and processes onsite.
*Capable of troubleshooting validation issues associated with projects, process development etc.
*Designs, implements and executes validation studies for manufacturing and control equipment.
*Provide technical assistance on current US FDA and EU validation requirements for Fill Finish manufacture and lyophilisation.
*Ensure that the validation status of equipment and systems are in compliance with cGMP at all times.
Experience:
*Science or Engineering qualification.
*Previous experience of working as a Senior Validation / Validation Engineer for a major pharmaceutical organisation.
*Key validation experience within compliance of equipment, systems and processes.
*5 years + experience working in a pharmaceutical Manufacturing Environment
*Sterile manufacturing experience is essential.
An excellent hourly rate is on offer alongside an exceptional opportunity to join a Global Market Leading Pharmaceutical organisation based in Ireland.
Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this long term contract opportunity.