Equipment Validation Specialist

Lonza is seeking an Equipment Validation Specialist, Level III to lead complex validation activities for biopharmaceutical manufacturing systems in a cGMP environment. In this role, you will plan and execute IQ/OQ/PQ, develop robust protocols and reports, manage risk assessments, and maintain lifecycle documentation for critical equipment and utilities. You will collaborate with engineering, manufacturing, and quality teams to support tech transfers, new product introductions, and inspections. …