Description
The GMP Associate I supports medical-device manufacturing by operating production equipment, packing finished products, loading automatic hoppers, assembling components, and resolving basic HMI faults. The role follows GMP, GDP, cleanroom, FDA, and ISO 13485 standards, participates in lean initiatives, and requires adherence to safety procedures, documentation, and cleanroom attire. The shift is 12 hours on a 2-2-3 schedule from 6:30 a.m. to 6:45 p.m., with a high school diploma or equivalent and prior manufacturing or production experience preferred.
