Description
A Global Market Leading Pharmaceutical organisation based in Ireland currently have a long term contract assignment for an experienced Validation Engineer.Working on a major investment programme within their state of the art 'sterile fill finish' facility we are looking for an experienced Validation Engineer with previous experience working within a sterile / fill finish environment.
Equipment will include: Autoclaves, Washers, dry heat oven, clean rooms, filling machines
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
*Ensure that the validation status of equipment and systems are in compliance with cGMP at all times.
Qualifications:
*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.
This is a 12-24 month contract assignment. Call me today for further information