Job Description
One of our large Medical Device companies is seeking a Validation Engineer to lead and support cross-functional validation and
implementation activities to qualify raw materials, processes, equipment, and systems,
ensuring timely execution and compliant documentation. Their responsibilities will include:
• Plan and execute multiple validation and implementation projects across
manufacturing platforms, from strategy through final report approval.
• Develop and qualify material, equipment, and process changes by authoring and
executing protocols (IQ/OQ/PQ) and documenting results against acceptance
criteria.
• Apply structured problem-solving (e.g., RCA/5-Why/FMEA) to investigate issues,
define corrective actions, and prevent recurrence during validation and routine
operations.
• Drive project management for qualification activities, including schedules,
risk/issue tracking, stakeholder updates, and readiness for approval.
• Ident...