Equipment Validation Engineer III - Biopharmaceutical Manufacturing
Lonza
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. This position offers exposure to advanced technologies, global projects, and a culture focused on innovation, quality, and patient impact.
Vacancy posted 1 day ago
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