Job DescriptionRole: Manager (M2) - Production NLocation: Pithampur Unit-3 NReports To: Senior Manager / Plant Production Head NExperience Required: Min 15 years in Pharmaceutical manufacturing with exposure to regulatory-approved facilities (USFDA, MHRA, EU, etc.). NSpecialization: Derma, Nasal, Liquid Oral dosage forms NEducation: Nn B.Pharm / M.Pharm N B.E. / B.Techn M.Sc. (Chemistry, Biotechnology, Pharmacy, or related disciplines) NnKey Expectations NProduction Managementn N Execute manufacturing and filling activities as per plan. N Achieve production targets and schedule adherence. N Ensure optimum utilization of manpower, equipment, materials, and utilities. N Handle SAP, Viva, eBMR/EBR, and PAS-X MES systems. NnQuality & Compliance Nn Ensure compliancewith cGMP, Data Integrity, and regulatory requirements. N Maintain audit readiness for USFDA, MHRA, EU, WHO, etc. N Manage deviations, investigations, CAPA, OOS/OOT, and market complaints. N Support validation, qualification, and technology transfer activities. NnOperational Excellence Nn Improve productivity, yield, and cycle times. N Drive Lean Manufacturing and Six Sigma initiatives. N Reduce manufacturing costs (COGM, CCPC). N Lead waste reduction and process optimization projects. NnEquipment & Facility Management Nn Ensure equipment reliability and uptime. N Coordinate preventive maintenance and breakdown management. N Support automation, digitization, and 21 CFR Part 11 compliance.



N Participate in expansion and modification projects. NnSafety & EHSn N Promote zero-accident culture. N Conduct risk assessments and incident investigations. N Drive safety observations and corrective actions. NnPeople Leadership Nn Develop production teams through training and coaching. N Conduct Gemba, SOP, andcapability-building sessions. N Manage performance, engagement, and succession planning. NnMajor KPIsnSafety Nn Zero Lost Time Accidents (LTA) N Near-miss reporting andclosure N Safety observation closure rate NnQualitynn Right First Time (RFT) N Deviation reduction N CAPA closure compliance N Audit observation management NnDeliverynn Schedule adherence N OTIF manufacturing performance N Batch release support timelines NnCostnn COGM reduction N CCPC reductionn Yield improvement N Cost-saving projects NnProductivityn N OEE improvementn Throughput enhancement N Cycle time reduction N Capacity utilization NnPeoplennTraining compliance N Attrition controln Succession readiness N Employee engagement NnTechnical Competencies Nn cGMP & RegulatoryCompliance N Investigation & CAPA N Validation & Qualification N Lean Manufacturing & Operational Excellence N Data Integrity & 21 CFRPart 11 N Risk Managementn NBehavioral Competencies Nn Leadership & TeamBuilding N Decision Makingn Problem Solving N Stakeholder Management N Communication Skills N Continuous Improvement Mindset N

📌 Manager (Indore GPO)
🏢 Lupin India
📍 Indore GPO