Job description

**Preferred candidate profile** - Hands-on experience in Semi-Solids, Oral Solids, Oral Liquids, External Liquids, and Packaging Operations. - Experience in WHO-GMP, EU-GMP regulated facilities preferred. - Develop and implement maintenance strategies to achieve maximum equipment availability and reliability. - Minimize machine downtime and improve OEE. - Manufacturing Equipment Maintenance related to Oral Solid Dosage (Tablets/Capsules), Semi-Solid Manufacturing, Oral Liquid Manufacturing, External Liquids/Shampoo Manufacturing, Dusting Powder Manufacturing, Filling & Packing Equipment Maintenance. - Ensure compliance with cGMP, WHO-GMP, MHRA, USFDA, EU GMP, and other applicable regulations. - Support regulatory inspections and client audits. - Maintain complete maintenance documentation. - Ensure compliance with data integrity requirements. - Participate in investigations, deviations, CAPA, and change controls. - Qualification & Validation Support of IQ/OQ/PQ Equipment Qualification Utility Qualification Requalification Programs FAT/SAT Activities New Project Equipment Installation - To handle Department related Statutory Compliances, Compliances for Quality Management System, and Compliances for EHS/EMS Management System. - Preferred good knowledge of Rapid Mixer Granulator (RMG), Fluid Bed Dryer (FBD),Coating Machines, Compression Machines, Capsule Filling Machines, Vibro Sifters Bin Blenders, Dust Extraction Systems