GMP Process Engineer & Validation Specialist
Keystone Industries
Keystone Industries is seeking a Process Engineer in Gibbstown, NJ to develop and optimize manufacturing processes for FDA-regulated products. You will support validation activities, write CAPAs and change controls, and collaborate with QA, production, engineering, analytical, and R&D teams to ensure quality and efficient production. Ideal candidates have 3-5 years of process engineering experience, knowledge of cGMP and ISO standards, and proficiency with validation plans and equipment #J-18808-Ljbffr Keystone Industries
Vacancy posted 4 days ago
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