Experience – REQUIRED 10 years’ experience in a Validation Role within a GMP Operating facility (Pharmaceuticals preferred). This project entails execution of the Validation Master Plan from writing protocols, execution of protocols and writing of summary reports. The validation efforts will entail processes, cleaning, facilities/utilities and laboratory. This validation project will commence in June/July timeframe thru the entire completion of the validation efforts.
Absolutely NO CONSIDERATION will be given unless you have the required experience necessary, then please forward your credentials to email@example.com for consideration on this validation project.