Description
Project Validation Engineer required to join a global pharmaceutical company located in south Ireland for a 12 month contract. The C&Q Engineer will have a key role in ensuring the on-going validation compliance of equipment, systems and processes in both solid dosage forms and sterile products manufacturing.
Role and responsibilities:
. 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 c GMP at all times.
Requirements:
. 3rd level Science or Engineering qualification.
. You will have 8-10 years experience working in a Healthcare Manufacturing Environment, ideally part of which would be in the pharmaceutical sector.
. Sterile experience preferred.
If this is you please apply today.