Our client is currently seeking Validation Engineers to assist with large ongoing 2-3 year projects. Main functions will consist of developing & authoring specifications or in-field execution of IQ/OQ/PQ and assisting with User Requirement Specifications (URS) while sending out drafts of URS and documentation. The consultants will not be running their own projects; however, they will be supporting PM’s in creating protocols to ensure projects & deliverables are completed on time. There are CIP skids, pumps, piping & tanking systems, mixers, and other equipment that will need to be validated for modifications as well as support within packaging IOQ as well.
Validation Engineering, Large-scale projects, IQ/OQ/PQ (authoring, development, execution), previous Pharma/Bio experience
Excellent communication skills in cross-functional collaborative team environment. Must work well & communicate effectively well with others
Plus/Nice to have (not required):
Cleaning validation, FDA cGMP, Capital Projects, Project Management
Experience outweighs degree
NY: Validation Engineer (232149)