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GUARDIAN DRUG COMPANY, INC. Validation Engineer in Dayton, New Jersey

Validation Engineer, Dayton, NJ: Perform qualification of pharmaceutical manufacturing and packaging equipment of oral solid dosage forms and facilities. Conduct calibration, preventive maintenance, and troubleshooting of automation systems and manufacturing and packaging equipment. Prepare, maintain, and review documentation, including SOPs, change control, product contact surface area specifications, engineering change notices, engineering drawings, validation protocols, and reports. Oversee utility operations, maintenance, and repairs, including Purified water systems, compressed air, HVAC equipment, and steam boilers. Manage or assist material and equipment selection, ordering, and delivery tracking during the facility or capacity expansion projects. Must have knowledge about pharmaceutical manufacturing processes, Fluid Mechanics, Design for Manufacturability, Thermodynamics, and Lean Manufacturing. Duties include working with Word, Excel, PowerPoint, and AutoCAD. Manage or assist material and equipment selection, ordering, and delivery tracking during the facility/capacity expansion projects. Master in Mechanical or Industrial or Production Engineering, or related. Mail resumes to Guardian Drug Company, 2 Charles Court, Dayton, NJ 08810, or email hr@guardiandrug.com. Refer VJP2025.

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