3+ years of experience working with, delivering, or supporting Validation applications for the manufacturing sector 3+ years of experience in the Pharma/Biotech, MedTech, or similarly regulated industry Knowledge of quality/manufacturing operations in the Pharma/Biotech and/or Medical Device/Diagnostics sectors Willingness to travel 20-30%, primarily in the EU (when possible) Excellent verbal and written communication, interpersonal, and presentation skills Energetic self-starter; able to work independently Understanding process design and Quality processes/operations Critical thinking and problem solving