Description
Our Medical Device/Pharmaceutical client has a contract requirement for an experienced Validation Engineer.We are looking for a Validaton Engineer with recent experience of working within a cGMP environment, to carry out the validation, execution and writing of protocols for API process equipment, clean rooms & utility systems.
This will include:
- Performing & reviewing vendor SAT's FAT's
- Creating executing protocols IQ OQ PQ
- Execution experience of API equipment such as: Reactors, Dryers, Centrifuge, IBC's etc
- Utility: Such as HVAC, GAS, AIR etc
- Any CSV would be advantageous as would electrical/I&C background